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三乙胺 → HCID 86609165,化合物

HRID 1161925
笔记
打印预览

反应方程式

HRID 1161925 反应方程式
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][C@H:14]([O:16][CH3:17])[CH2:13][C@H:12]1[C:18]#[N:19])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH2:21][OH:22].C(N(CC)CC)C>C(O)C>[CH2:1]([O:8][C:9]([N:11]1[CH2:15][C@H:14]([O:16][CH3:17])[CH2:13][C@H:12]1[C:18]([NH2:19])=[N:21][OH:22])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

5

反应物 3

HCID 8471三乙胺HCID 443297盐酸羟胺HCID 23626151benzyl-(2S,4R)-2-cyano4-methoxypyrrolidine-1-carboxylate

产物 1

HCID 86609165HCID 86609165,化合物

试剂、催化剂与溶剂 1

HCID 702乙醇溶剂

反应条件

温度
40 °C

实验过程

To benzyl-(2S,4R)-2-cyano-4-methoxypyrrolidine-1-carboxylate, dissolved in ethanol (0.4 M), hydroxylamine hydrochloride (1.3 eq.) and triethylamine (1.5 eq.) were added. The mixture was stirred at 40° C. for 4 hours then at room temperature overnight. The mixture was concentrated in vacuo and the residue dissolved in ethyl acetate washed with brine, dried over Na2SO4, filtered and concentrated to give title compound.

后处理

  1. customat room temperature
  2. customovernight
  3. concentrationThe mixture was concentrated in vacuo
  4. dissolutionthe residue dissolved in ethyl acetate
  5. washwashed with brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated

来源与证据

ORD记录
ord-4055fc0e09104c6ab869580f65e50008
来源数据集
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
专利号
US07820660B2

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记