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14-methyl-6,17,18-trioxatricyclo[10.3.2.11,12 ]octadecane | 65033-42-3

中文名称
——
中文别名
——
英文名称
14-methyl-6,17,18-trioxatricyclo[10.3.2.11,12 ]octadecane
英文别名
14-Methyl-16,17,18-trioxatetracyclo<10.3.2.11,12>octadecan;14-Methyl-16,17,18-trioxatetracylo<10.3.2.11.12>octadecan;14-Methyl-16,17,18-trioxatricyclo[10.3.2.11,12]octadecane;14-methyl-16,17,18-trioxatricyclo[10.3.2.11,12]octadecane
14-methyl-6,17,18-trioxatricyclo[10.3.2.1<sup>1,12</sup> ]octadecane化学式
CAS
65033-42-3
化学式
C16H28O3
mdl
——
分子量
268.397
InChiKey
DBYBXCCZGYEZMN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    19
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    14-methyl-6,17,18-trioxatricyclo[10.3.2.11,12 ]octadecane氢气 、 sodium hydroxide 作用下, 以 甲醇 为溶剂, 70.0 ℃ 、2.0 MPa 条件下, 反应 18.0h, 生成 3-methyl-1,5-dihydroxycyclopentadecane
    参考文献:
    名称:
    [EN] PROCESS FOR PREPARING 3-METHYLCYCLOPENTADECANE-1,5-DIOL
    [FR] PROCÉDÉ DE PRÉPARATION DE 3-MÉTHYLCYCLOPENTADÉCANE-1,5-DIOL
    摘要:
    本发明涉及通过对14-甲基-16,17,18-三氧杂三环[10.3.2.1]十八烷(II)进行氢解反应制备3-甲基环戊十五烷-1,5-二醇(I)的方法。本发明还涉及一种制备3-甲基环戊十五烷-1,5-二醇的方法,该方法是一种大环二元醇,可以作为制备大环香精如麝香酮和麝香内酯的前体。
    公开号:
    WO2017050713A1
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文献信息

  • [EN] SYNTHESIS OF 14-METHYL-16-OXABICYCLO[10.3.1]HEXADEC-12-ENE<br/>[FR] SYNTHÈSE DE 14-MÉTHYL-16-OXABICYCLO [10.3.1] HEXADÉC-12-ÈNE
    申请人:INT FLAVORS & FRAGRANCES INC
    公开号:WO2020150454A1
    公开(公告)日:2020-07-23
    Disclosed is a scalable process for preparation of 14-methyl-16-oxabicyclo[10.3.1]hexadec-12-ene (BCE), a key intermediate for manufacture of fragrance ingredient 3-methylcyclopentadecenone (MUSCENONE®) and analogs through reaction of 3-Methyl-1,5-cyclopentadecanedione (MCPD) and analogs with a metal or metalloid alkoxide in high yield and purity.
    本发明公开了一种可扩展的制备14-甲基-16-氧杂双环[10.3.1]十六烷-12-烯(BCE)的过程,该过程通过将3-甲基-1,5-环戊二酮(MCPD)和类似物与金属或类金属烷氧基反应,高产率高纯度制备香料成分3-甲基环戊十五烯酮(MUSCENONE®)和类似物的关键中间体。
  • Process for preparing 3-methylcyclopentadecane-1,5-diol
    申请人:BASF SE
    公开号:US10196332B2
    公开(公告)日:2019-02-05
    The present invention relates to a process for preparing 3-methylcyclopentadecane-1,5-diol (I) by hydrogenolysis of 14-methyl-16,17,18-trioxatricyclo[10.3.2.1]octadecane (II). The invention further relates to a process for preparing 3-methylcyclopentadecane-1,5-diol is a macrocyclic diol that can serve as precursor for a macrocyclic odorant, such as muscone and muscenone.
    本发明涉及一种通过氢解 14-甲基-16,17,18-三氧杂三环[10.3.2.1]十八烷(II)制备 3-甲基环十五烷-1,5-二醇(I)的工艺。本发明还涉及一种制备 3-甲基环十五烷-1,5-二醇的工艺,这种大环二醇可作为大环气味剂(如麝香酮和麝香草烯酮)的前体。
  • PROCESS FOR PREPARING 3-METHYLCYCLOPENTADECANE-1,5-DIOL
    申请人:BASF SE
    公开号:EP3353141B1
    公开(公告)日:2019-11-06
  • SYNTHESIS OF 14-METHYL-16-OXABICYCLO[10.3.1]HEXADEC-12-ENE
    申请人:International Flavors & Fragrances Inc.
    公开号:EP3911656A1
    公开(公告)日:2021-11-24
  • [EN] PROCESS FOR PREPARING 3-METHYLCYCLOPENTADECANE-1,5-DIOL<br/>[FR] PROCÉDÉ DE PRÉPARATION DE 3-MÉTHYLCYCLOPENTADÉCANE-1,5-DIOL
    申请人:BASF SE
    公开号:WO2017050713A1
    公开(公告)日:2017-03-30
    The present invention relates to a process for preparing 3-methylcyclopentadecane-1,5-diol (I) by hydrogenolysis of 14-methyl-16,17,18-trioxatricyclo[10.3.2.1]octadecane (II). The invention further relates to a process for preparing 3-methylcyclopentadecane-1,5-diol is a macrocyclic diol that can serve as precursor for a macrocyclic odorant, such as muscone and muscenone.
    本发明涉及通过对14-甲基-16,17,18-三氧杂三环[10.3.2.1]十八烷(II)进行氢解反应制备3-甲基环戊十五烷-1,5-二醇(I)的方法。本发明还涉及一种制备3-甲基环戊十五烷-1,5-二醇的方法,该方法是一种大环二元醇,可以作为制备大环香精如麝香酮和麝香内酯的前体。
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同类化合物

青蒿氧烷 甲基3-甲基-1,2,4-三氧杂环戊烷-3-羧酸酯 烯丙基苯臭氧化物 5-乙酰基-3,5-二甲基-1,2,4-三氧杂环戊烷-3-甲腈 3-苯基-1,2,4-三氧杂螺[5.4]癸烷 3-甲基-3-苯基-1,2,4-三氧杂螺[5.4]癸烷 3,5-二苯基-1,2,4-三氧杂环戊烷 3,3-二丁基-1,2,4-三氧杂螺[5.4]癸烷 1-异丙基-4-甲基-2,3,7-三氧杂双环[2.2.1]庚烷 1-(5-甲氧基-3-甲基-1,2,4-三四氢呋喃-3-基)乙酮 1-(5,5-二甲基-1,2,4-三四氢呋喃-3-基)乙酮 1-(3,5,5-三甲基-1,2,4-三四氢呋喃-3-基)乙酮 1,2,4-三噁戊环,3-(1-氯乙烯基)- cis-1,4-Dimethyl-2,3,17-trioxabicyclo<12.2.1>heptadecane trans-1,4-Dimethyl-2,3,17-trioxabicyclo<12.2.1>heptadecane adamantane-2-spiro-3'-8'-hydroxy-8'-methyl-1',2',4'-trioxaspiro[4.5]decane adamantane-2-spiro-3'-8'-hydroxy-1',2',4'-trioxaspiro[4.5]decane (3-methyl-1,2,4-trioxolan-3-yl)hexanal (3-methyl-5-phenyl-5-trifluoromethyl-1,2,4-trioxolan-3-yl)pentanal trioxolane 7 3-tert-butyl-3-methyl-5-phenyl-5-trifluoromethyl-1,2,4-trioxolane 3-Cyano-5-cyclohexyl-3-isobutyl-1,2,4-trioxolane 5'-Cyano-5'-isobutylspiro (trans-5-cyano-5-phenyl-1,2,4-trioxolan-3-yl)-3-cyclopentanecarbaldehyde 5'-Cyano-5'-phenylspiro 3-Cyano-3,5-diphenyl-1,2,4-trioxolane 3-Cyano-3-phenyl-5-tert-butyl-1,2,4-trioxolane 3-tert-Butyl-3-methyl-1,2,4-trioxaspiro[5.4]decane (trans-5-cyano-3,5-dimethyl-1,2,4-trioxolan-3-yl)hexanal (trans-5-cyano-5-methyl-1,2,4-trioxolan-3-yl)hexanal 3,5-dimethyl-5-(3-oxopropyl)-1,2,4-trioxolane-3-carbonitrile (trans-5-cyano-5-methyl-1,2,4-trioxolan-3-yl)pentanal 3-Cyano-3-methyl-5-phenyl-1,2,4-trioxolane 3-Cyano-5-cyclohexyl-3-methyl-1,2,4-trioxolane (E)-3-methyl-5-[7-oxohept-5-enyl]-1,2,4-trioxolane-3-carbonitrile (Z)-3-methyl-5-[5-oxopent-1-enyl]-1,2,4-trioxolane-3-carbonitrile (E)-3-methyl-5-[6-oxohex-4-enyl]-1,2,4-trioxolane-3-carbonitrile 3-methyl-5-[(E)-5-oxopent-3-enyl]-1,2,4-trioxolane-3-carbonitrile (Z)-3-methyl-5-[4-methyl-7-oxohept-3-enyl]-1,2,4-trioxolane-3-carbonitrile 3-(Chloromethyl)-3-methoxy-1,2,4-trioxolane cis-3,5-bis-(chloromethyl)-3,5-dimethoxy-1,2,4-trioxolane trans-3,5-bis-(chloromethyl)-3,5-dimethoxy-1,2,4-trioxolane cis-adamantane-2-spiro-3'-8'-[[(4'-formyl-1'-piperazinyl)carbonyl]methyl]-1',2',4'-trioxaspiro[4.5]decane adamantane-2-spiro-3’-8’-hydroxymethyl-1’,2’,4’-trioxaspiro[4,5]decane 3-(Chloromethyl)-3-fluoro-1,2,4-trioxolane trans-3,5-Bis(chloromethyl)-3-fluoro-1,2,4-trioxolane methyl spiro3,7>decane-2,3'-<1,2,4>trioxolane>-5'-carboxylate 3-Cyano-3-phenyl-1,2,4-trioxolane 3-ethyl-1,24-trioxolane dispiro[adamantane-2,2'-[1,3,5]trioxolane-4',1''-cyclohexane]-3''-ol