Tetrabutylammonium Hydroxide → 2-Vinylthio-4,5-bis-(p-methoxyphenyl)-thiazole

HRID 544669ノート

反応式

HRID 544669 の反応式
Br[CH2:2][CH2:3][S:4][C:5]1[S:6][C:7]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[C:8]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)[N:9]=1.[OH-].C([N+](CCCC)(CCCC)CCCC)CCC>C1(C)C=CC=CC=1.O>[CH:3]([S:4][C:5]1[S:6][C:7]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[C:8]([C:10]2[CH:11]=[CH:12][C:13]([O:16][CH3:17])=[CH:14][CH:15]=2)[N:9]=1)=[CH2:2]

参加物

5

実験手順

0.8 g of 2-(2-bromoethylthio)-4,5-bis-(p-methoxyphenyl)-thiazole are dissolved in 20 ml of toluene. 2 ml of a 30% strength solution of tetrabutylammonium hydroxide in water are added and the mixture is heated under reflux for 2 hours while stirring vigorously. The mixture is then allowed to cool, the organic phase is separated off, washed twice with 10 ml of water each time, dried over sodium sulphate and concentrated to dryness by evaporation. The crude product is purified by chromatography over a silica gel column with toluene/ethyl acetate (10:1) as eluant. The fractions that according to the thin layer chromatogram contain 2-vinylthio-4,5-bis-(p-methoxyphenyl)-thiazole are concentrated by evaporation and dried to constant weight. 2-Vinylthio-4,5-bis-(p-methoxyphenyl)-thiazole is obtained in the form of a pale yellow oil.

後処理

  1. temperaturethe mixture is heated
  2. temperatureunder reflux for 2 hours
  3. temperatureto cool
  4. customthe organic phase is separated off
  5. washwashed twice with 10 ml of water each time
  6. dry with materialdried over sodium sulphate
  7. concentrationconcentrated to dryness by evaporation
  8. customThe crude product is purified by chromatography over a silica gel column with toluene/ethyl acetate (10:1) as eluant
  9. concentrationare concentrated by evaporation
  10. customdried to constant weight

出典と根拠

ORDレコード
ord-eea933dc5ca04b2d8539151a8cd9ee0a
出典データセット
uspto-grants-1984_05
特許番号
US04451471

反応ノート

読み込み中…