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Bromoacetyl bromide → Acetamide, 2-bromo-N-methyl-N-2-propynyl-

HRID 1973324
ノート
印刷プレビュー

反応式

HRID 1973324 の反応式
[CH3:1][NH:2][CH2:3][C:4]#[CH:5].[Br:6][CH2:7][C:8](Br)=[O:9].C(=O)(O)[O-].[Na+]>C(Cl)Cl.C(OCC)C>[CH3:1][N:2]([CH2:3][C:4]#[CH:5])[C:8](=[O:9])[CH2:7][Br:6]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 61147Bromoacetyl bromideHCID 96160N-methylpropyn-2-ylamineHCID 516892Sodium Bicarbonate

生成物 1

HCID 10774018Acetamide, 2-bromo-N-methyl-N-2-propynyl-収率 85%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒2 回HCID 6344Dichloromethane溶媒
2 回

反応条件

温度
25 °C

実験手順

A solution of 13.8 g (0.2 mol) of N-methylpropargylamine in 20 ml methylene chloride was added dropwise to a stirred and cooled (below 15° C) solution of 40.2 g (0.2 mol bromoacetyl bromide and 16 g (0.2 mol) sodium bicarbonate in 250 ml methylene chloride. The reaction mixture was allowed to warm to about 25° C and stirred for 2 hours. The reaction mixture was then filtered and evaporated under reduced pressure to give an oily residue. The residue was diluted with 150 ml ethyl ether to form a two-phase mixture consisting of an ether phase and a dark oil. The ether phase was separated, dried over magnesium sulfate, and evaporated to give 32.3 g of N-methyl-N-propargyl-alpha-bromoacetamide.

後処理

  1. stirringstirred for 2 hours
  2. filtrationThe reaction mixture was then filtered
  3. customevaporated under reduced pressure
  4. customto give an oily residue
  5. customto form a two-phase mixture
  6. customThe ether phase was separated
  7. dry with materialdried over magnesium sulfate
  8. customevaporated

出典と根拠

ORDレコード
ord-87137ed9e7814607b0e727ce3196f3a8
出典データセット
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03997326

反応ノート

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