化工社
首页MCP工作台Skills
首页工作台通知我的
llms.txt · MCP 指南隐私政策 · 服务条款 · 支持v1.8.0
  1. 首页
  2. /反应

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → (2S,3S)-2-[Cbz(methyl)amino]-3-methylpentanal

HRID 74716
笔记
打印预览

反应方程式

HRID 74716 反应方程式
[CH2:1]([O:8][C:9](=[O:19])[N:10]([C@@H:12]([C@@H:15]([CH3:18])[CH2:16][CH3:17])[CH2:13][OH:14])[CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.O.COC(C)(C)C>CS(C)=O>[CH3:11][N:10]([C@@H:12]([C@@H:15]([CH3:18])[CH2:16][CH3:17])[CH:13]=[O:14])[C:9](=[O:19])[O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=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

6

反应物 4

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 8471三乙胺HCID 15413甲基叔丁基醚HCID 11777636(2S,3S)-2-[Cbz(methyl)amino]-3-methylpentan-1-ol

产物 1

HCID 10378073(2S,3S)-2-[Cbz(methyl)amino]-3-methylpentanal收率 87%

试剂、催化剂与溶剂 1

HCID 679二甲基亚砜
溶剂

反应条件

温度
0 °C

实验过程

To a solution of #1 (8.27 g, 31.2 mmol, 1 eq.) in dimethyl sulfoxide (41.35 mL, 0.75 M), was added triethylamine (8.70 mL, 64.0 mmol, 2.05 eq.) and the mixture was cooled to 0° C. Sulfur trioxide pyridine complex (10.18 g, 63.96 mmol, 2.05 eq.) was then added portion-wise, while keeping the internal temperature below 8° C. The reaction was allowed to reach room temperature and was stirred for 18 hours. The reaction was poured into water (100 mL) and tert-butyl methyl ether (100 mL). The aqueous layer was back-extracted with tert-butyl methyl ether (50 mL) and the combined organic layers were washed with brine (100 mL), dried over magnesium sulfate, filtered, concentrated in vacuo and purified by silica gel chromatography (Gradient: 10% to 60% ethyl acetate in heptane) to provide #2 (7.14 g, 87%) as a colorless oil. 1H NMR (400 MHz, DMSO-d6), presumed to be a mixture of rotamers, characteristic signals: δ 9.61 (s, 1H), 7.26-7.42 (m, 5H), 5.01-5.13 (m, 2H), 4.04-4.12 (m, 1H), 2.86 and 2.82 (2 s, total 3H), 1.94-2.11 (br m, 1H), 1.26-1.42 (br m, 1H).

后处理

  1. additionSulfur trioxide pyridine complex (10.18 g, 63.96 mmol, 2.05 eq.) was then added portion-wise
  2. customthe internal temperature below 8° C
  3. customto reach room temperature
  4. extractionThe aqueous layer was back-extracted with tert-butyl methyl ether (50 mL)
  5. washthe combined organic layers were washed with brine (100 mL)
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. custompurified by silica gel chromatography (Gradient: 10% to 60% ethyl acetate in heptane)

来源与证据

ORD记录
ord-333b239e60d947ca9d346a6a12d1bc1f
来源数据集
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08828401B2

反应笔记

加载中…

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