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Hydrochloric Acid → 1-(5-Bromo-2,4-difluorophenyl)ethan-1-one

HRID 1471436
ノート
印刷プレビュー

反応式

HRID 1471436 の反応式
[Al+3].[Cl-].[Cl-].[Cl-].[Br:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:7]=1[F:13].[C:14](Cl)(=[O:16])[CH3:15].Cl>CCOC(C)=O>[Br:5][C:6]1[C:7]([F:13])=[CH:8][C:9]([F:12])=[C:10]([C:14](=[O:16])[CH3:15])[CH:11]=1
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 313Hydrochloric AcidHCID 6367Acetyl chlorideHCID 676741-Bromo-2,4-difluorobenzeneHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 207853591-(5-Bromo-2,4-difluorophenyl)ethan-1-one

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
60 °C

実験手順

A mixture of AlCl3 (1040 g, 7878.7 mmol) in 1-bromo-2,4-difluorobenzene ([CAS 348-57-2], 600 g, 3108.9 mmol) was stirred for 10 min at 60° C. Acetyl chloride [CAS 75-36-5], 366 g, 4662.4 mmol) was added dropwise in the reaction mixture for 4 h at 60° C. The mixture was stirred an additional 6 h at 95° C. The reaction mixture was cooled to −10° C. Ice (2450 g) was added for 1.5 h. HCl (12 N, 1500 mL) was added and the mixture was stirred for 1 h. EtOAc (9000 mL) was added and the organic layer was washed with water, dried over Na2SO4 and filtered. After concentration, the residue was purified by column chromatography over silica gel (eluent: petroleum ether/EtOAc, 50/1) to yield I-18 (300 g, 41%).

後処理

  1. stirringThe mixture was stirred an additional 6 h at 95° C
  2. temperatureThe reaction mixture was cooled to −10° C
  3. stirringthe mixture was stirred for 1 h
  4. washthe organic layer was washed with water
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationAfter concentration
  8. customthe residue was purified by column chromatography over silica gel (eluent: petroleum ether/EtOAc, 50/1)
  9. customto yield I-18 (300 g, 41%)

出典と根拠

ORDレコード
ord-7fdaceea662c407090d79150dfbc0472
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09012448B2

反応ノート

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