CAS: 6476-36-4; Triisopropylphosphine

该化合物是有机磷原子三异丙基化合物,其特征为三异丙基化合物,在室内温度下,黄黄色液体无色,以其强烈的核生殖特性而著称,使它成为各种化学反应中的有用螺旋,特别是在过渡性金属催化中,大异丙基化合物组的存在会造成不耐烦,从而影响与三异丙基硫酸一起形成的金属复合体的再活动性和选择性;这种化合物在有机溶剂中溶解,在标准条件下相对稳定,但可能对氧化敏感;三异丙基磷经常用于有机合成,特别是在形成磷氧化物和制造以磷为基础的催化剂方面;此外,它也会在有机金属化学领域发挥作用,并可在某些反应中起到减少剂的作用;在处理该化合物时,应注意安全防范措施,因为如果吸入或吸入,可能会对健康造成危害.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

2-iodo-propane di-isopropylphosphine isopropylmagnesium bromide dithi°Carboxy-triisopropyl-phosphonium betaine5-phosphanylidene)-eth-(E)-ylidene]-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-amine[2-Phenyl-2-(triisopropyl-λ5-phosphanylidene)-eth-(E)-ylidene]-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-amine phosphoniumbromidTriisopropyl(pentafluorphenyl)methylphosphoniumbromid trimethylphosphane diisopropylmethylphosphine

合成工艺路线路线简述

  • 合成目标产物 Triisopropylphosphine 主要起始原料 Triisopropylphosphonium Tetrafluoroborate
  • (文献来源)合成步骤主要原料 Triisopropylphosphonium Tetrafluoroborate
📜异丙基溴化镁置于三氯化磷体系中,化学反应生成 三异丙基膦
参考文献:苯硫酸铜锌和第一种硒酸铜锌和碲酸铜配合物的合成及晶体结构
标题:苯硫酸铜锌和第一种硒酸铜锌和碲酸铜配合物的合成及晶体结构
摘要:五铜锌苯基硫属元素络合物 [(Ipr3Pcu)3(Znme2)2(Sph)3] (1),[(Ipr3Pcu)2(Znph)4(Sph)6] (2),[(Ipr3Pcu)2(Znet)4 (Sph)6] (3),[(Ipr3Pcu)3(Znet)(Seph)4] (4) 和 [(Ipr3Pcu)3Cu(Ipr3Pzn)(Teph)6] (5) 是由膦反应合成的稳定的苯基硫属元素铜配合物与 Znr2 (R = Me,Et,Ph) 有和没有额外的硫属元素醇.通过单晶x射线结构分析和核磁共振光谱对新型混合金属化合物进行了表征.图 4 和图 5 分别是具有 Zn-Se-Cu 或 Zn-Te-Cu 键的化合物的第一个例子.
DOI:10.1002/zaac.201600426

专利信息


专利号:US-6504041-B2
优先权日:1996-11-15
标题 :Synthesis of ruthenium or osmium metathesis catalysts
发明人:GRUBBS ROBERT H; BELDERRAIN TOMAS R; BROWN SETH N; WILHELM THOMAS E
权利人:CALIFORNIA INST OF TECHN
摘要:The present invention relates to the synthesis of highly active ruthenium and osmium carbene metathesis catalyst in good yield from readily available starting materials. The catalysts that may be synthesized are of the general formula n wherein: n M is ruthenium or osmium; n X and X 1 are independently any anionic ligand; n L and L 1 are any neutral electron donor ligand; and, n R and R 1 are each hydrogen or one of the following substituent groups: C 2 -C 20 alkenyl, C 2 -C 20 alkynyl, C 1 -C 20 alkyl, aryl, C 1 -C 20 carboxylate, C 1 -C 20 alkoxy, C 2 -C 20 alkenyloxy, C 2 -C 20 alkynyloxy, aryloxy, C 2 -C 20 alkoxycarbonyl, C 1 -C 20 alkylthio, C 1 -C 20 alkylsulfonyl and C 1 -C 20 alkylsulfinyl. Optionally, the substituent group may be substituted with one or more groups selected from C 1 -C 5 alkyl, halogen, C 1 -C 5 alkoxy, and aryl. When the substitute aryl group is phenyl, it may be further substituted with one or more groups selected from a halogen, a C 1 -C 5 alkyl, or a C 1 -C 5 alkoxy. Specific synthetic protocols for vinyl alkylidene catalysts wherein R is hydrogen and R 1 is —CHCR 12 R 13 and non-vinyl alkylidene catalysts are also disclosed. In addition to the ease of synthesis (typically a one-step synthesis), the reactions generally may be run at or above room temperature and the resulting products usually may be used without extensive post synthesis purification.

专利号:US-7102023-B2
优先权日:1999-11-24
标 题:Protecting groups useful in the synthesis of polysaccharides, natural products, and combinatorial libraries
发明人:BUCHWALD STEPHEN L; PLANTE OBADIAH J; SEEBERGER PETER H
权利人:MASSACHUSETTS INST TECHNOLOGY
摘要:One aspect of the present invention relates to optionally substituted halogenated benzyl halides and the like. These compounds are useful as halogenated benzyl ether-based protecting groups for a variety of functional groups. Another aspect of the present invention relates to use of said protecting groups in an orthogonal protecting group strategy for the synthesis of complex molecules that comprise a number of suitable functional groups. Another aspect of the present invention relates to saccharides bearing various arrays of protecting groups of the present invention. Another aspect of the present invention relates to a method of synthesizing an oligosaccharide or glycoconjugate, comprising the steps of: using a saccharide bearing at least one protecting group of the present invention to glycosylate a second molecule to give a product comprising said saccharide; and removing a protecting group of the present invention from said product.

专利号:US-6613910-B2
优先权日:2001-04-02
标题 :One-pot synthesis of group 8 transition metal carbene complexes useful as olefin metathesis catalysts
发明人:GRUBBS ROBERT H; MORGAN JOHN P; BENITEZ DIEGO; LOUIE JANIS
权利人:CALIFORNIA INST OF TECHN
摘要:The invention provides a novel method for synthesizing transition metal carbene complexes useful as olefin metathesis catalysts. The method is a convenient one-pot synthesis in which transition metal carbenes are prepared in high yield from readily available starting materials via a dihydrogen complex containing two different anionic ligands, preferably a phosphine and a heteroatom-stabilized carbene. The invention additionally provides a method for synthesizing precursors to carbene ligands useful, inter alia, in the aforementioned one-pot synthesis. The precursors are in the form of trichloromethyl adducts of the formula L 1 -CCl 3 , where L 1 is a heteroatom-stabilized carbene ligand, and are prepared by contacting an unsaturated, ionized analog of L-CCl 3 with a non-nucleophilic base in the presence of chloroform.

专利号:US-10173993-B2
优先权日:2015-12-09
标题 :Process for the synthesis of sulfones and sulfonamides
发明人:VON WOLFF NIKLAS; CHAR JOËLLE; CANTAT THIBAULT
权利人:COMMISSARIAT ENERGIE ATOMIQUE
摘要:A one pot single step process is described for the synthesis of a compound, including a labeled compound, containing a sulfonyl functional group comprising the step of mixing together a silane, an SO 2 source, an electrophilic compound, an activating compound and optionally a metal catalyst. A process for producing tracers from a labeled sulfonyl containing compound prepared by the described process is also included.

专利号:US-5789530-A
优先权日:1996-12-20
标 题:Catalyzed synthesis of aramid from carbon monoxide, aromatic dichlorides, and diamines
发明人:SEN AYUSMAN; KIM JANG SUB
权利人:PENN STATE RES FOUND
摘要:The synthesis of an aramid by the catalyzed reaction of carbon monoxide, an aromatic dichloride, such as 1,4-dichlorobenzene, and a diamine, such as 1,4-diaminobenzene, is disclosed. The reaction may be catalyzed by palladium (II) and palladium (0)-containing catalysts with chelating trialkyl phosphines, such as bis(diisopropylphosphino)-propane.

专利号:US-7034096-B2
优先权日:2002-02-19
标题:Ring-expansion of cyclic olefins metathesis reactions with an acyclic diene
发明人:CHOI TAE-LIM; LEE CHOON WOO; KIM HYUNJIN M; GRUBBS ROBERT H
权利人:CALIFORNIA INST OF TECHN
摘要:This invention relates generally to synthetic procedures that include the step of ring-opening metathesis of cyclic olefins and reaction with an acyclic diene co-reactant to produce olefin macrocycles by ring expansion, or alternatively. The ring expansion of the cyclic olefin is provided by three types of sequential olefin metathesis (ring-opening, cross, and ring-closing olefin metathesis). More particularly, the invention pertains to synthesis of olefin macrocycles via olefin metathesis reactions using a Group 8 transition metal complex as the metathesis catalyst. Macrocycles provided herein have a variety of uses in the pharmaceutical, biomedical, organic synthesis and chemical industries, such as the production of crown ethers that are useful as metal complexing species.

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主要参考文献

参考标题:Synthesis Of Esters By Functionalisation Of Co2
摘要:The Invention Relates To A Method For (I) Producing A Carboxylic Ester Of Formula (I). Said Method Comprises The Steps Of: A) Bringing An Organosilane/borane Of Formula Si Or B Into Contact With Co 2 , In The Presence Of A Catalyst And An Electrophilic Compound Of Formula (III), The Groups R 1 , R 2 , R 3 , R 4 , R 5 , Y, And M′ Being As Defined In Claim 1; And Optionally B) Recovering The Compound Of Formula (I) Produced.

合成参考文献


摘要:Ogasawara, M., Science of Synthesis, (2008) 44, 62.
摘要:de Meijere, A.; Kozhushkov, S. I., Science of Synthesis, (2009) 48, 558.
摘要:Vrána, J.; Růžička, A., Science of Synthesis Knowledge Updates, (2021) 2, 29.
摘要:Podlech, J., Science of Synthesis Knowledge Updates, (2018) 4, 199.
摘要:Nakao, Y., Science of Synthesis: Special Topics, (2022) 1, 566.
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