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Trichloroacetyl chloride → N-(3-chloro)allyl-N-methoxyethyl trichloroacetamide

HRID 34507
ノート
印刷プレビュー

反応式

HRID 34507 の反応式
[Cl:1][CH:2]=[CH:3][CH2:4][NH:5][CH2:6][CH2:7][O:8][CH3:9].C(N(CC)CC)C.[Cl:17][C:18]([Cl:23])([Cl:22])[C:19](Cl)=[O:20]>ClCCl>[Cl:1][CH:2]=[CH:3][CH2:4][N:5]([CH2:6][CH2:7][O:8][CH3:9])[C:19](=[O:20])[C:18]([Cl:23])([Cl:22])[Cl:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6420Trichloroacetyl chlorideHCID 8471TriethylamineHCID 85568957N-(3-chloro)allyl-N-methoxyethylamine

生成物 1

HCID 54017101N-(3-chloro)allyl-N-methoxyethyl trichloroacetamide収率 92.7%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

N-(3-chloro)allyl-N-methoxyethylamine (2.25 g, 0.015 mol) and 1.52 g (0.015 mol) triethylamine were stirred in 70 ml dichloromethane. The reaction was kept at approximately 5° C. with an ice-water bath. Trichloroacetyl chloride (2.73 g, 0.015 mol) in 10 ml dichloromethane was added dropwise to the cooled solution. Upon completion of the addition, the mixture was stirred at room temperature for 6 hours. The reaction mixture was then washed twice with saturated brine and dried with sodium sulfate. Rotary evaporation yielded 4.1 g of the above-named product.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe reaction was kept at approximately 5° C. with an ice-water bath
  2. additionUpon completion of the addition
  3. washThe reaction mixture was then washed twice with saturated brine
  4. dry with materialdried with sodium sulfate
  5. customRotary evaporation

出典と根拠

ORDレコード
ord-8acb45df98e14c3a9a8f3a881c597456
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04762548

反応ノート

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