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N,N-二甲基甲酰胺 → 2-Azido-1-(4-methylsulfanyl-phenyl)-ethanone

HRID 1908252
笔记
打印预览

反应方程式

HRID 1908252 反应方程式
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([S:11][CH3:12])=[CH:7][CH:6]=1)=[O:4].CN(C=O)C.[N-:18]=[N+:19]=[N-:20].[Na+]>CCOC(C)=O>[N:18]([CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([S:11][CH3:12])=[CH:7][CH:6]=1)=[O:4])=[N+:19]=[N-:20]
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 6228N,N-二甲基甲酰胺HCID 33557叠氮化钠HCID 27375232-溴-4'-甲硫基苯乙酮

产物 1

HCID 161273432-Azido-1-(4-methylsulfanyl-phenyl)-ethanone收率 100%

试剂、催化剂与溶剂 1

HCID 8857乙酸乙酯溶剂

反应条件

温度
15 °C

实验过程

A solution consisting of 2-bromo-1-(4-methylsulfanyl-phenyl)-ethanone (2.00 g, 8.16 mmol) and DMF (7 mL) was cooled to 15° C. and treated portion-wise with sodium azide (583 mg, 8.98 mmol). Once addition was complete, the reaction mixture was stirred for 3 h with gradual warming to rt. The reaction mixture was then diluted with EtOAc (20 mL) and washed with water (25 mL×2), NaHCO3 (satd., 25 mL×2), and brine. The combined organic phases were dried (Na2SO4) and concentrated to dryness to yield the title compound (1.69 g, 100%).

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

后处理

  1. additionOnce addition
  2. temperaturewith gradual warming to rt
  3. washwashed with water (25 mL×2), NaHCO3 (satd., 25 mL×2), and brine
  4. dry with materialThe combined organic phases were dried (Na2SO4)
  5. concentrationconcentrated to dryness

来源与证据

ORD记录
ord-6bbde4efda324d1bb92722c4b543e8d2
来源数据集
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08598202B2

反应笔记

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