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Hydrochloric Acid → 2-Chloro-4,5-difluorobenzoic acid

HRID 982202
ノート
印刷プレビュー

反応式

HRID 982202 の反応式
C[C:2]([C:4]1[C:9]([Cl:10])=[CH:8][C:7]([F:11])=[C:6]([F:12])[CH:5]=1)=[O:3].Cl[O-:14].[Na+].Cl>C(Cl)Cl>[Cl:10][C:9]1[CH:8]=[C:7]([F:11])[C:6]([F:12])=[CH:5][C:4]=1[C:2]([OH:3])=[O:14]
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 313Hydrochloric AcidHCID 27364892'-Chloro-4',5'-difluoroacetophenoneHCID 23665760Sodium Hypochlorite

生成物 1

HCID 7371712-Chloro-4,5-difluorobenzoic acid収率 85.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To 19.1 g (0.1 mol) of 2-chloro-4,5-difluoroacetophenone, 280.4 g (0.4 mol) of a 12% sodium hypochlorite aqueous solution was added, and the mixture was reacted under reflux for 4 hours. After cooling, concentrated hydrochloric acid was dropwise added thereto until the pH became 1. The formed white crystals were dissolved in methylene chloride and separated from the aqueous phase. The separated aqueous phase was extracted twice with methylene chloride, and the extracts were added to the oil phase. Then, the solvent was distilled off to obtain 16.4 g (yield: 85.1%) of 2-chloro-4,5-difluorobenzoic acid as white crystal.

後処理

  1. customthe mixture was reacted
  2. temperatureunder reflux for 4 hours
  3. temperatureAfter cooling
  4. customseparated from the aqueous phase
  5. extractionThe separated aqueous phase was extracted twice with methylene chloride
  6. additionthe extracts were added to the oil phase
  7. distillationThen, the solvent was distilled off

出典と根拠

ORDレコード
ord-2199b81e01a4403496d56bafff43b122
出典データセット
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04994610

反応ノート

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