CAS: 1113-78-6; Tris(1-Methylpropyl)Borane

该化合物是有机体化合物,其特征是附于一个对子原子的三组1-甲基丙基化合物,该化合物一般是一种无色液体,以其反应性为名,特别是在有机金属化学方面;它是各种合成应用中的一种有用的试剂,包括水合反应,它可以将双环结合成有机有机物;1体聚体组群的存在,会给化学反应带来不耐烦,影响其再活动性和选择性;Tris(1-甲基丙基)borane由于它能够稳定某些蚂蚁,并且由于对金的电不灵性,可以作为刘易斯酸;在处理该化合物时,安全防范至关重要,因为它可能会对有机物化合物造成典型的危害,包括易燃性和接触时潜在的健康风险.

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

(Z)-2-Butene butene-2 sodium tri-sec-butylborohydride bis(N,N-dimethylamino)chlorophosphine (3,3-Dimethyl-1-butenyliden)cyclohexan 4-methyl-1-phenylhexa-1,2-diene 3,4,5-trimethylheptan-4-ol

合成工艺路线路线简述

    📜2-丁烯置于硼烷体系中,用 四氢呋喃 用作溶剂,化学反应生成三仲丁基硼烷
    参考文献:Reaction Of Organoboranes With 2-Bromoacrolein. A Facile One-Stage Synthesis Of .Alpha.-Bromo Aldehydes
    标题:Reaction Of Organoboranes With 2-Bromoacrolein. A Facile One-Stage Synthesis Of .Alpha.-Bromo Aldehydes
    摘要:
    Doi:10.1021/ja01017A049

    海关参考信息

    专利信息


    专利号:US-7247752-B2
    优先权日:2004-10-01
    标 题 :Methods for the synthesis of astaxanthin
    发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID
    权利人:CARDAX PHARMACEUTICALS INC
    摘要:A method used for synthesizing intermediates for use in the synthesis of carotenoids and carotenoid analogs, and/or carotenoid derivatives. In some embodiments, the invention includes methods for synthesizing optically active intermediates useful for the synthesis of optically active carotenoids. Synthesis of optically active carotenoids, in one embodiment, may be accomplished by forming an optically active dihydroxy intermediate from ketoisopherone. The optically active dihydroxy intermediate may be converted into optically active astaxanthin derivatives.

    专利号:US-8222458-B2
    优先权日:2008-06-13
    标题 :Process or synthesis of (3S)- and (3R)-3-hydroxy-beta-ionone, and their transformation to zeaxanthin and beta-cryptoxanthin
    发明人:KHACHIK FREDERICK; CHANG AN-NI
    权利人:KHACHIK FREDERICK; CHANG AN-NI; UNIV MARYLAND
    摘要:Disclosed is a process for the synthesis of (3R)-3-hydroxy-β-ionone and its (3S)-enantiomer in high optical purity from commercially available (rac)-α-ionone. The key intermediate for the synthesis of these hydroxyionones is 3-keto-α-ionone ketal that was prepared from (rac)-α-ionone after protection of this ketone as a 1,3-dioxolane. Reduction of 3-keto-α-ionone ketal followed by deprotection, lead to 3-hydroxy-α-ionone that was transformed into (rac)-3-hydrox-β-ionone by base-catalyzed double bond isomerization in 46% overall yield from (rac)-α-ionone. The racemic mixture of these hydroxyionones was then resolved by enzyme-mediated acylation in 96% ee. (3R)-3-Hydroxy-β-ionone and its (3S)-enantiomer were respectively transformed to (3R)-3-hydroxy-(β-ionylideneethyl)triphenylphosphonium chloride [(3R)-C 15 -Wittig salt] and its (3S)-enantiomer [(3S)-C 15 -Wittig salt] according to known procedures. Double Wittig condensation of these Wittig salts with commercial available 2,5- dimethtylocta-2,4,6-triene-1,8-dial provided all 3 stereoisomers of zeaxanthin. Similarly, (3R)-C 15 -Wittig and its (3S)-enantiomer were each coupled with β-apo-12′-carotenal.

    专利号:US-7858828-B2
    优先权日:2008-03-26
    标 题 :Process for synthesis of (3R,3'R,6'R)-lutein and its stereoisomers
    发明人:KHACHIK FREDERICK; CHANG AN-NI
    权利人:UNIV MARYLAND
    摘要:(3R,3′R,6′R)-Lutein and (3R,3′R)-zeaxanthin are two dietary carotenoids that are present in most fruits and vegetables commonly consumed in the US. These carotenoids accumulate in the human plasma, major organs, and ocular tissues. In the past decade, numerous epidemiological and experimental studies have shown that lutein and zeaxanthin play an important role in the prevention of age-related macular degeneration (AMD) that is the leading cause of blindness in the U.S. and Western World. The invention provides a process for the synthesis of (3R,3′R,6′R)-lutein and its stereoisomers from commercially available (rac)-α-ionone by a C 15 +C 10 +C 15 coupling strategy. In addition, the present invention also provides access to the precursors of optically active carotenoids with 3-hydroxy-ε-end group that are otherwise difficult to synthesize. The process developed for the synthesis of lutein and its stereoisomers is straightforward and has potential for commercialization.

    专利号:US-4427587-A
    优先权日:1982-11-10
    标 题:Total synthesis of antitumor antibiotics BBM-2040A and BBM-2040B
    发明人:KANEKO TAKUSHI; WONG HENRY S L
    权利人:BRISTOL MYERS CO
    摘要:A new chemical synthesis of the pyrrolobenzodiazepine antibiotics BBM-2040A and B is disclosed. The disclosed total synthesis uses readily available starting materials and provides a useful alternative to the microbiological procedure previously used to prepare these antibiotics.

    专利号:WO-2023152730-A1
    优先权日:2022-02-14
    标题 :Amine-borane adducts in the synthesis of polyester and its copolymers using cyclic esters and compositions thereof
    发明人:FENG XIAOSHUANG; LIU JINGJING; GNANOU YVES
    权利人:UNIV KING ABDULLAH SCI & TECH
    摘要:Embodiments of the present disclosure provide for the process of synthesis of polyester and its copolymers through (co)polymerization of cyclic esters and with other oxygenated monomers using amine-borane adduct. Embodiments of the present disclosure further describe the controlled anionic ring-opening polymerization of the cyclic compounds. Embodiments of the present disclosure also describe the polymerization of cyclic compounds using the synergistic effect of amines and thioureas. Embodiments of the present disclosure also describe compositions of polymers formed by the said process.

    专利号:US-7452994-B2
    优先权日:2001-09-12
    标 题 :Synthesis of enantiomerically pure amino-substituted fused bicyclic rings
    发明人:MCEACHERN ERNEST J; BRIDGER GARY J; SKUPINSKA KRYSTYNA A; SKERLJ RENATO T; YANG WEN
    权利人:ANORMED INC
    摘要:This invention describes various processes for synthesis and resolution of racemic amino-substituted fused bicyclic ring systems. One process utilizes selective hydrogenation of an amino-substituted fused bicyclic aromatic ring system. An alternative process prepares the racemic amino-substituted fused bicyclic ring system via nitrosation. In addition, the present invention describes the enzymatic resolution of a racemic mixture to produce the (R)- and (S)-forms of amino-substituted fused bicyclic rings as well as a racemization process to recycle the unpreferred enantioner. Further provided by this invention is an asymmetric synthesis of the (R)- or (S)-enantiomer of primary amino-substituted fused bicyclic ring systems.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Toyota, S.; Iwanaga, T., Science of Synthesis, (2010) 45, 802.
    摘要:Kostikov, R. R.; Khlebnikov, A. F.; Sokolov, V. V., Science of Synthesis, (2010) 47, 866.
    摘要:Zaidlewicz, M.; Krzemiński, M. P.; Dzieleńdziak, A., Science of Synthesis, (2009) 48, 373.
    摘要:Kantchev, E. A. B.; Organ, M. G., Science of Synthesis, (2009) 48, 10.
    摘要:Kimura, T., Science of Synthesis Knowledge Updates, (2016) 2, 446.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知