CAS: 817-60-7; 2-Ethylheptan-1-Ol

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    2-ethylheptanoic acid formaldehyd 2-ethyl-1-hexene 3,6-diethyltetrahydro-2H-pyran-2-one 2-ethylheptanoic acid 2-ethylheptanal

    合成工艺路线路线简述

    • 合成目标产物 2-Ethylheptan-1-Ol 主要起始原料 2-Ethylheptanoic Acid
    • (文献来源)合成步骤主要原料 2-Ethylheptanoic Acid
    📜3-Ethyl-5-Prop-(E)-Ylidene-5H-Furan-2-One置于(Acetylacetonato)Dicarbonylrhodium (L),Palladium On Activated Charcoal,Molybdenum Hexacarbonyl 氢气体系中,用 四氢呋喃,1,4-二氧六环 作为反应溶剂,60.0~180.0 °C,15.0 Mpa 条件下,反应 5.0H,反应生成 2-乙基庚烷-1-醇
    参考文献:羧酸和内酯的双金属催化还原为醇和二醇
    标题:羧酸和内酯的双金属催化还原为醇和二醇
    摘要:研究了氢对羧酸的均相催化还原反应.由第8族或第9组晚过渡金属和第二族第6或7组过渡金属羰基组成的双金属催化剂具有协同作用,可在中等条件下以高收率转化.除了不同催化剂前体的影响外,还研究了温度,氢气压力和催化剂浓度的影响.[rh(acac)(co)2]和[mo(co)6的等摩尔混合物]显示出最高的活性,因此适用于将内酯还原为二醇.发现催化剂的还原电势取决于所用内酯的环大小.五元环内酯几乎不转化为二醇,而六元和七元环内酯则容易反应.
    DOI:10.1002/1615-4169(200207)344:5<525::Aid-Adsc525>3.0.Co;2-U

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    专利信息


    专利号:US-10000432-B2
    优先权日:2014-01-13
    标 题 :Processes for the synthesis of chiral 1-alkanols
    发明人:NEGISHI EI-ICHI
    权利人:PURDUE RESEARCH FOUNDATION
    摘要:The invention relates to highly enantioselective processes for the synthesis of chiral 1-alkanols via Zr-catalyzed asymmetric carboalumination of alkenes.

    专利号:US-4167513-A
    优先权日:1977-09-06
    标题 :Synthesis of unsaturated esters and lactone from butadiene and carbon dioxide
    发明人:MUSCO ALFREDO; SANTI ROBERTO; CHIUSOLI GIAN P
    权利人:MONTEDISON SPA
    摘要:Octadienyl esters of 2-ethylidene-hepta-3,5-dienoic and 2-vinyl-hepta-3,5-dienoic acids of formula C 8 H 11 COOC 8 H 13 and δ-lactone of formula ##STR1## or 2-ethylidene-hepta-6-ene-5-olide, are prepared by reaction of 1,3-butadiene with CO 2 at a temperature comprised between about 20° and 150° C. and at a total pressure between about 10 and 500 atm in the presence of a phosphinic complex of palladium having the formula Pd[P(R) 3 ] x , wherein x is an integer from 2 to 4, and (R) 3 is a homogeneous or heterogeneous group consisting of alkyls, cycloalkyls having up to 8 carbon atoms and of phenyls, also substituted, in an inert atmosphere. n The obtained products are 'per se' new and are valuable intermediates for synthesis of chemicals (fungicides, pesticides, etc.) and in particular as effective plasticizers.

    专利号:US-4451679-A
    优先权日:1982-10-21
    标题 :Alcohols and aldehydes prepared from olefins and synthesis gas
    发明人:KNIFTON JOHN F; LIN JIANG-JEN; GRIGSBY JR ROBERT A; BRADER JR WALTER H
    权利人:TEXACO INC
    摘要:This invention concerns a process of preparing alcohols and aldehydes which comprises the steps of contacting a mixture of terminal and/or internal olefins and synthesis gas with a catalyst system comprising a ruthenium-containing compound dispersed in a low melting quaternary phosphonium or ammonium base or salt and heating said resultant reaction mixture under a pressure of 100 psi or greater at a temperature of at least 50 DEG C. for a sufficient time to produce said alcohols and aldehydes.

    专利号:US-4469895-A
    优先权日:1982-10-21
    标题 :Process for preparing alcohols from olefins and synthesis gas
    发明人:KNIFTON JOHN F; GRIGSBY JR ROBERT A
    权利人:TEXACO INC
    摘要:This invention concerns an improved process of preparing predominantly linear alcohols which comprises the steps of contacting a mixture of terminal and/or internal olefins and synthesis gas with a catalyst system comprising a ruthenium-containing compound in conjunction with one or more tertiary amine promoters, dispersed in a low melting quaternary phosphonium salt and heating said resultant reaction mixture under a pressure of 100 psi or greater at a temperature of at least 50 DEG C. for a sufficient time to produce said alcohols.

    专利号:EP-3679005-A2
    优先权日:2017-06-12
    标 题 :Synthesis of building blocks and feedstocks for manufacturing renewable polymers

    专利号:EP-3094613-A1
    优先权日:2014-01-13
    标题:Processes for the synthesis of chiral 1-alkanols

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/bf02036741
    摘要:Southwell IA, Maddox CDA, Zalucki MP. Metabolism of 1,8-cineole in tea tree (Melaleuca alternifolia andM. linariifolia) by pyrgo beetle (Paropsisterna tigrina). Journal of Chemical Ecology. 1995 Apr;21(4):439–53. doi: 10.1007/bf02036741.
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