2-Chloroethanol → 1-[Bis(4-fluorophenyl)methoxy]-2-chloroethane

HRID 35296

反応式

HRID 35296 の反応式
[Cl:1][CH2:2][CH2:3][OH:4].S(=O)(=O)(O)O.[F:10][C:11]1[CH:16]=[CH:15][C:14]([CH:17]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][CH:20]=2)O)=[CH:13][CH:12]=1.O>C1C=CC=CC=1>[Cl:1][CH2:2][CH2:3][O:4][CH:17]([C:14]1[CH:15]=[CH:16][C:11]([F:10])=[CH:12][CH:13]=1)[C:19]1[CH:20]=[CH:21][C:22]([F:25])=[CH:23][CH:24]=1

参加物

6

反応物 4

HCID 342-ChloroethanolHCID 962WaterHCID 1118Sulfuric AcidHCID 1230494,4'-Difluorobenzhydryl alcohol

生成物 1

HCID 107793021-[Bis(4-fluorophenyl)methoxy]-2-chloroethane

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

A mixture of 20 parts of 2-chloroethanol, 3 parts of sulfuric acid and 16 parts of benzene was heated on a water-bath. Then there were added dropwise 35 parts of 4-fluoro-α-(4-fluorophenyl)benzenemethanol dissolved in 32 parts of benzene. After the addition was complete, the whole was stirred and refluxed for 4 hours. After cooling the reaction mixture was poured into water. The benzene layer was separated, dried over calcium chloride and evaporated. The residue was distilled in vacuo, yielding 35 parts of 1,1'-[(2-chloroethoxy)methylene]bis[4-fluorobenzene]; bp. 164°-166° C. at 1.5 mm. pressure; nD20 : 1.5462; d2020 : 1.2290 (intermediate 1).

後処理

  1. temperaturewas heated on a water-bath
  2. additionAfter the addition
  3. temperaturerefluxed for 4 hours
  4. temperatureAfter cooling the reaction mixture
  5. customThe benzene layer was separated
  6. dry with materialdried over calcium chloride
  7. customevaporated
  8. distillationThe residue was distilled in vacuo

出典と根拠

ORDレコード
ord-aa649f34fbe0408682aae1bc3a34ceb5
出典データセット
uspto-grants-1988_08
特許番号
US04766125

関連ノート

読み込み中…