摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(S)-5-(benzyloxy)-1,1,1-trifluoro-5-methyl-2-(naphthalen-3-yl)hex-3-yn-2-ol | 1255152-67-0

中文名称
——
中文别名
——
英文名称
(S)-5-(benzyloxy)-1,1,1-trifluoro-5-methyl-2-(naphthalen-3-yl)hex-3-yn-2-ol
英文别名
(2S)-1,1,1-trifluoro-5-methyl-2-naphthalen-2-yl-5-phenylmethoxyhex-3-yn-2-ol
(S)-5-(benzyloxy)-1,1,1-trifluoro-5-methyl-2-(naphthalen-3-yl)hex-3-yn-2-ol化学式
CAS
1255152-67-0
化学式
C24H21F3O2
mdl
——
分子量
398.425
InChiKey
JOQZQLPEVYOXRZ-HSZRJFAPSA-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:
    29
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    (S)-5-(benzyloxy)-1,1,1-trifluoro-5-methyl-2-(naphthalen-3-yl)hex-3-yn-2-ol2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 6.0h, 以100%的产率得到(S)-1,1,1-trifluoro-5-methyl-2-(naphthalen-3-yl)hex-3-yne-2,5-diol
    参考文献:
    名称:
    Cinchona Alkaloid-Catalyzed Asymmetric Trifluoromethylation of Alkynyl Ketones with Trimethylsilyl Trifluoromethane
    摘要:
    The first catalytic enantioselective trifluoromethylation of alkynyl ketones 1 with (trifluoromethyl)trimethylsilane is disclosed by an operationally simple procedure, based on the combination of ammonium bromide of bis-cinchona alkaloids with Me4NF to afford trifluoromethyl-substituted tertiary propargyl alcohols (up to 96% ee), which are the important chiral building blocks for pharmaceuticals. Biologically attractive aryl heteroaryl trifluoromethyl carbinols were also synthesized.
    DOI:
    10.1021/ol102189c
  • 作为产物:
    描述:
    4-(benzyloxy)-4-methyl-1-(naphthalen-3-yl)pent-2-yn-1-one(三氟甲基)三甲基硅烷 在 2Br(1-)*C46H52N4O2(2+)四甲基氟化铵四丁基氟化铵 作用下, 以 二氯甲烷甲苯四氢呋喃 为溶剂, 反应 3.0h, 生成 (S)-5-(benzyloxy)-1,1,1-trifluoro-5-methyl-2-(naphthalen-3-yl)hex-3-yn-2-ol 、 (R)-5-(benzyloxy)-1,1,1-trifluoro-5-methyl-2-(naphthalen-3-yl)hex-3-yn-2-ol
    参考文献:
    名称:
    Cinchona Alkaloid-Catalyzed Asymmetric Trifluoromethylation of Alkynyl Ketones with Trimethylsilyl Trifluoromethane
    摘要:
    The first catalytic enantioselective trifluoromethylation of alkynyl ketones 1 with (trifluoromethyl)trimethylsilane is disclosed by an operationally simple procedure, based on the combination of ammonium bromide of bis-cinchona alkaloids with Me4NF to afford trifluoromethyl-substituted tertiary propargyl alcohols (up to 96% ee), which are the important chiral building blocks for pharmaceuticals. Biologically attractive aryl heteroaryl trifluoromethyl carbinols were also synthesized.
    DOI:
    10.1021/ol102189c
点击查看最新优质反应信息