Water → 1-(3-Bromo-2-hydroxy-5-methylphenyl)ethan-1-one

HRID 1042523ノート

反応式

HRID 1042523 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10].[Br:12]Br.O>ClCCl.[Fe]>[Br:12][C:7]1[C:2]([OH:1])=[C:3]([C:9](=[O:11])[CH3:10])[CH:4]=[C:5]([CH3:8])[CH:6]=1

参加物

6

反応物 3

HCID 962WaterHCID 150682-Hydroxy-5-methylacetophenoneHCID 24408Bromine

生成物 1

HCID 111389181-(3-Bromo-2-hydroxy-5-methylphenyl)ethan-1-one収率 48%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of 21.5 g (0.143 mol) of 20 in 40 mL of dry dichloromethane, 0.3 g of iron turnings was added, and then a solution of 10.7 mL (34.2 g, 0.215 mol) of bromine in 100 mL of dichloromethane was added dropwise by vigorous stirring for 20 min. This mixture was refluxed for 30 min, and then 300 mL of water was added. The organic layer was separated, and the aqueous layer was extracted with 2×100 mL of dichloromethane. The combined organic extract was washed by saturated aqueous Na2SO3, dried over K2CO3, and then evaporated to dryness. Rectification of the residue in vacuum gave 15.7 g (48%) of the title product (bp 105-115° C./1 mm).

後処理

  1. temperatureThis mixture was refluxed for 30 min
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with 2×100 mL of dichloromethane
  4. extractionThe combined organic extract
  5. washwas washed by saturated aqueous Na2SO3
  6. dry with materialdried over K2CO3
  7. customevaporated to dryness

出典と根拠

ORDレコード
ord-cb559e5603004aa794e67acf466603f6
出典データセット
uspto-grants-2013_10
特許番号
US08557936B2

反応ノート

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