CAS: 613-31-0; 9,10-Dihydroanthracene

该化合物是多环芳烃衍生物,其特点是部分氢化的炭疽结构,该化合物被广泛用作有机合成的前体,特别是在染料,光导体和功能材料的生产中.其饱和中心环在保持9和10位置的回活动的同时,增强了稳定性,使其对选择性功能化很有价值.复合物展品有利于热和氧化性稳定性,适合需要受控再活动的应用.此外,它还作为氢化和脱氢过程机械学研究的示范基体.其定义明确的化学特性和多功能使它在学术和工业研究环境中成为可靠的中间体.

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CAS号120-12-7 蒽 | CAS号84-65-1 蒽醌 | CAS号1586-00-1 2-苄基苯甲醇 | CAS号1564-64-3 9-溴蒽 | CAS号90-44-8 蒽酮 | CAS号85-52-9 邻苯甲酰苯甲酸 | CAS号100-51-6 苯甲醇 | CAS号108-67-8 均三甲苯 | CAS号4985-70-0 1-氯蒽 | CAS号1689-64-1 9-芴醇 | CAS号3073-51-6 9-(9-hydroxyflu... | CAS号111410-41-4 9-(9,10-dihydro... | CAS号1499-00-9 2-苯基氮丙啶 | CAS号3278-14-6 N-苯乙基-苯甲酰胺 | CAS号128600-81-7 9-(2-Benzamido-... | CAS号22020-69-5 2,5-diphenyl-4,... | CAS号4957-14-6 二对甲苯基甲烷 | CAS号120-12-7 蒽

合成工艺路线路线简述

    📜蒽醌置于苯基膦体系中,化学反应 72.0H,以91%的收率获得产物9,10-二氢蒽
    参考文献:用苯基膦还原芳香酮或硫酮
    标题:用苯基膦还原芳香酮或硫酮
    摘要:某些芳族酮或硫酮与苯基膦反应并随后加入二乙基二硫化物得到酮和 S,S-二乙基苯基二硫代膦酸酯或 S,S-二乙基苯基膦酰三硫代酯的还原产物.膦部分的可能中间体被认为是苯基亚膦基[php=o]或苯基亚膦硫基[php=s].10,10'-联蒽酮和δ10,10'-联蒽酮的还原分别导致碳-碳单键和双键的断裂和羰基的还原.
    DOI:10.1246/bcsj.58.2577

    海关参考信息

    专利信息


    专利号:US-8889897-B2
    优先权日:2011-12-23
    标 题:Electrocarboxylation synthesis for obtaining intermediates useful for the synthesis of SPAN derivatives
    发明人:OSSO J ORIOL; VEGA LOURDES F; GALLARDO ILLUMINADO; GUIRADO GONZALO; GOMEZ ANA BELEN; RECHE FRANCISCA IRENE
    权利人:AIR PROD & CHEM
    摘要:The present invention relates to a process for obtaining a compound of formula (1), (2) or (3) by means of a electrocarboxylation with CO 2 . The present invention also relates to the new intermediates (1) and (2). The present invention further relates to the use of intermediates (1) and (2) as starting materials for the synthesis of SPAN derivatives.

    专利号:US-7632975-B2
    优先权日:2004-12-22
    标 题:Process for the synthesis of arylfluorenes and analogs thereof
    发明人:HEIDENHAIN SOPHIE
    权利人:CDT OXFORD LTD
    摘要:A process is provided for the synthesis of a compound of formula (I): n nwherein:n M=0 or 1; N and p are 0 or 1 to 4; X is a single bond, O, S or NH; And R 1 -R 4 are as defined in claim 1.

    专利号:US-8785664-B2
    优先权日:2010-02-11
    标 题 :Process for the preparation of nebivolol
    发明人:BARTOLI SANDRA; CIPOLLONE AMALIA; FATTORI DANIELA
    权利人:MENARINI INT OPERATIONS LU SA
    摘要:The present invention relates to a novel process for the synthesis of Nebivolol product represented in Scheme (1), comprised of a reduced number of high-yield steps, and characterized by the kinetic resolution of the two epoxide pairs diastereoisomeric therebetween (mixture 1), allowing to avoid complex chromatographic separations.

    专利号:US-8487122-B2
    优先权日:2010-02-11
    标题 :Process for the preparation of nebivolol
    发明人:BARTOLI SANDRA; CIPOLLONE AMALIA; FATTORI DANIELA
    权利人:BARTOLI SANDRA; CIPOLLONE AMALIA; FATTORI DANIELA; MENARINI INT OPERATIONS LU SA
    摘要:The present invention relates to a novel process for the synthesis of Nebivolol product represented in Scheme (1), comprised of a reduced number of high-yield steps, and characterized by the kinetic resolution of the two epoxide pairs diastereoisomeric therebetween (mixture 1), allowing to avoid complex chromatographic separations.

    专利号:US-3980706-A
    优先权日:1975-11-06
    标 题:Synthesis of 2,7-bisdimethylamino-10-P-dimethylaminophenyl-9,10-dihydro-9,9-dimethylanthracene
    发明人:MONDRON PETER J
    权利人:HORIZONS INC
    摘要:The preparation of leucodihydroanthracenes represented by the general formula ##SPC1## n Wherein each of Z and Z' is selected from the group consisting of H and dialkylamino, and at least one Z is dialkylamino and each Q is selected from the group consisting of H and alkyl (C 1 -C 4 ) and Z' is selected from the group consisting of aryl, alkyl and H, the preferred Z' being ##SPC2##

    专利号:US-4921955-A
    优先权日:1987-11-06
    标 题 :Process for the synthesis of 1-substituted imidazole-5-carboxylic acids and carboxylic acid derivatives
    发明人:TOEPFL WERNER
    权利人:CIBA GEIGY CORP
    摘要:The invention relates to a process for the preparation of 1,5-disubstituted imidazoles of the formula (I) by alkylation of an N-cyanoformamidine of the formula II X-NH-CH=N-CH (II) to form an N,N-disubstituted N'-cyanoformamidine of the formula (IV) which is cyclised under the action of bases to form a 4-aminoimidazole of the formula (V) and then reduced to form the product of the formula I. The invention relates also to a special process for the reduction of the aminoimidazole V to I, and to intermediate compounds for carrying out this process and to processes for the preparation of the intermediate compounds. The meaning of the substituents X and L is explained in detail in the text.

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    📌 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:Toyota, S.; Iwanaga, T., Science of Synthesis, (2010) 45, 810.
    摘要:Chciuk, T. V.; Flowers, R. A.; Flowers, R. A., Science of Synthesis Knowledge Updates, (2016) 2, 245.
    摘要:Dai, X.; Shi, F., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 145.
    摘要:Flowers, R. A., II; Chciuk, T. V.; Bartulovich, C. O., Science of Synthesis, (2020) , 90.
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