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Water → HCID 67310078、化合物

HRID 2192359
ノート
印刷プレビュー

反応式

HRID 2192359 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[O:5][CH2:6][CH2:7][NH2:8].C(=O)([O-])[O-].[K+].[K+].[Br:18][CH2:19][C:20](Br)=[O:21].O>ClCCl>[Br:18][CH2:19][C:20]([NH:8][CH2:7][CH2:6][O:5][C:4]1[CH:9]=[CH:10][CH:11]=[C:2]([F:1])[CH:3]=1)=[O:21]
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 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 61147Bromoacetyl bromideHCID 142453302-(3-Fluorophenoxy)ethan-1-amine

生成物 1

HCID 67310078HCID 67310078、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

A mixture of 2-(3-fluorophenoxy)ethylamine (0.93 g) and potassium carbonate (1.24 g in dichloromethane (20 mL) at 0° C. was treated with bromoacetyl bromide (1.04 mL). The reaction mixture was stirred at 0° C. for 30 mins then at room temperature for 6 h. Water was added and the mixture was stirred until effervescence ceased. The organic layer was separated and the organic layer was evaporated to afford the crude product which was purified by silica gel chromatography eluting with 0-50% EtOAc/pentane to give the sub-titled compound (1.17 g) as a brown oil.

後処理

  1. waitat room temperature for 6 h
  2. stirringthe mixture was stirred until effervescence
  3. customThe organic layer was separated
  4. customthe organic layer was evaporated
  5. customto afford the crude product which
  6. customwas purified by silica gel chromatography
  7. washeluting with 0-50% EtOAc/pentane

出典と根拠

ORDレコード
ord-eef35d60839c43fa8cc3f38cf74ee82d
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08329729B2

反応ノート

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