N-bromobutanimide → Methyl alpha-bromo-2-chlorophenylacetate

HRID 66290

反応式

HRID 66290 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([O:11][CH3:12])=[O:10].[Br:13]N1C(=O)CCC1=O>Br.C(Cl)(Cl)(Cl)Cl>[Br:13][CH:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[Cl:1])[C:9]([O:11][CH3:12])=[O:10]

参加物

5

反応物 2

HCID 67184N-bromobutanimideHCID 93683Methyl (2-chlorophenyl)acetate

生成物 1

HCID 10730282Methyl alpha-bromo-2-chlorophenylacetate

試薬・触媒・溶媒 2

HCID 260Hydrogen Bromide触媒HCID 5943Carbon Tetrachloride溶媒

実験手順

A stirred mixture of 36.9 g of methyl o-chlorophenylacetate, 36.0 g of N-bromosuccinimide, and 2 drops of 48% hydrobromic acid in 500 ml of carbon tetrachloride is refluxed for 20 hours and then filtered through magnesium silicate. Evaporation under reduced pressure gives methyl α-bromo-o-chlorophenylacetate as a straw-colored liquid.

後処理

  1. temperatureis refluxed for 20 hours
  2. filtrationfiltered through magnesium silicate
  3. customEvaporation under reduced pressure

出典と根拠

ORDレコード
ord-c8f5c52d90874291ad7a6c0fa5ef5b8f
出典データセット
uspto-grants-1978_12
特許番号
US04131611

関連ノート

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