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(2R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentan-1-ol | 1242057-49-3

中文名称
——
中文别名
——
英文名称
(2R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentan-1-ol
英文别名
——
(2R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentan-1-ol化学式
CAS
1242057-49-3
化学式
C15H30O3
mdl
——
分子量
258.401
InChiKey
HLIFUKJBFIXNPL-POQQGIQPSA-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):
    3.5
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (2R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentan-1-ol2-碘酰基苯甲酸 作用下, 以 四氢呋喃二甲基亚砜 为溶剂, 反应 2.0h, 以92%的产率得到(2R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentanal
    参考文献:
    名称:
    Synthesis of C15–C27 segment of venturicidine X by utilizing desymmetrization protocol
    摘要:
    We have achieved the synthesis of C15-C27 fragment of venturicidine X using desymmetrization protocol, substrate-controlled Grignard reaction, Barton-McCombie reaction, Sharpless epoxidation, and TBSOTf-mediated rearrangement to produce the aldol product through a non-aldol route as the key step following 23 longest linear sequences with 6.4% overall yield starting from a known intermediate 11. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.05.148
  • 作为产物:
    描述:
    tert-butyl-[(2R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentoxy]-dimethylsilane四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以91%的产率得到(2R,4R)-4-[(4S,5R,6S)-6-ethyl-2,2,5-trimethyl-1,3-dioxan-4-yl]-2-methylpentan-1-ol
    参考文献:
    名称:
    Synthesis of C15–C27 segment of venturicidine X by utilizing desymmetrization protocol
    摘要:
    We have achieved the synthesis of C15-C27 fragment of venturicidine X using desymmetrization protocol, substrate-controlled Grignard reaction, Barton-McCombie reaction, Sharpless epoxidation, and TBSOTf-mediated rearrangement to produce the aldol product through a non-aldol route as the key step following 23 longest linear sequences with 6.4% overall yield starting from a known intermediate 11. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.05.148
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文献信息

  • Synthesis of C15–C27 segment of venturicidine X by utilizing desymmetrization protocol
    作者:J.S. Yadav、Sk. Samad Hossain、Debendra K. Mohapatra
    DOI:10.1016/j.tetlet.2010.05.148
    日期:2010.8
    We have achieved the synthesis of C15-C27 fragment of venturicidine X using desymmetrization protocol, substrate-controlled Grignard reaction, Barton-McCombie reaction, Sharpless epoxidation, and TBSOTf-mediated rearrangement to produce the aldol product through a non-aldol route as the key step following 23 longest linear sequences with 6.4% overall yield starting from a known intermediate 11. (C) 2010 Elsevier Ltd. All rights reserved.
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