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Sodium Hydroxide → 1,2-Difluoro-4,5-dimethylbenzene

HRID 613806
ノート
印刷プレビュー

反応式

HRID 613806 の反応式
Cl[C:2]1([F:12])[CH2:7][C:6]([CH3:8])=[C:5]([CH3:9])[CH2:4][C:3]1(F)[F:10].[OH-].[Na+]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1>[F:10][C:3]1[CH:4]=[C:5]([CH3:9])[C:6]([CH3:8])=[CH:7][C:2]=1[F:12]
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

4

反応物 2

HCID 14798Sodium HydroxideHCID 195936835-Chloro-1,2-dimethyl-4,4,5-trifluorocyclohexene

生成物 1

HCID 142277911,2-Difluoro-4,5-dimethylbenzene

試薬・触媒・溶媒 1

HCID 66133Benzyl triethylammonium chloride触媒

反応条件

温度
80 °C

実験手順

To a stirred solution of 5-chloro-1,2-dimethyl-4,4,5-trifluorocyclohexene of 12.6 g prepared in Example 14 was added 1.0 g of benzyltriethylammonium chloride, and then the reaction mixture was heated to 80° C. followed by slowly adding 40 g of 50% aqueous sodium hydroxide solution for 30 min. The reaction mixture was stirred for additional 2 hours at 80° C., and then the resultant was purified by steam distillation followed by separating the aqueous layer. The organic layer was dried with calcium chloride, and then 7.3 g of the desired product was collected by fractional distillation at temperature 150° C. as a colorless liquid.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. distillationthe resultant was purified by steam distillation
  2. customby separating the aqueous layer
  3. dry with materialThe organic layer was dried with calcium chloride
  4. distillation7.3 g of the desired product was collected by fractional distillation at temperature 150° C. as a colorless liquid

出典と根拠

ORDレコード
ord-d168ffdbc1464913baf518db1544ccdc
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06008407

反応ノート

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