Water → (4-Methoxyphenyl)[5-[(phenylmethyl)thio]-2-thienyl]methanone

HRID 1153787ノート

反応式

HRID 1153787 の反応式
[CH2:1]([SH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].Br[C:12]1[S:13][C:14]([C:17](=[O:26])[C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[CH:15][CH:16]=1.O>CN(C=O)C>[CH2:1]([S:8][C:12]1[S:13][C:14]([C:17](=[O:26])[C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[CH:15][CH:16]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

反応条件

温度
25 °C

実験手順

Benzyl mercaptan (1.24 g, 0.01 mol) was added to a stirred mixture of sodium hydride (50% oil dispersion, 0.44 g, 0.11 mol) and degassed DMF (10 mL). The resulting mixture was warmed cautiously until gas evolution ceased. After cooling to 25° C., a solution of 2-bromo-5-(4-methoxybenzoyl)thiophene (2.97 g, 0.01 mol) in DMF (10 mL) was added dropwise. After complete addition, the mixture was heated on the steam bath for 2.5 hours and poured into waTER (200 mL). The aqueous mixture was extracted with ether (2×200 mL) and the extracts were washed with water, saturated NaCl solution and dried (Na2SO4). After evaporation of the solvent, the residue was collected with the aid of hexane and dried, 1.98 g, m.p. 103°-105° C.

後処理

  1. customdegassed DMF (10 mL)
  2. temperatureThe resulting mixture was warmed cautiously until gas evolution
  3. additionAfter complete addition
  4. temperaturethe mixture was heated on the steam bath for 2.5 hours
  5. extractionThe aqueous mixture was extracted with ether (2×200 mL)
  6. washthe extracts were washed with water, saturated NaCl solution
  7. dry with materialdried (Na2SO4)
  8. customAfter evaporation of the solvent
  9. customthe residue was collected with the aid of hexane
  10. customdried

出典と根拠

ORDレコード
ord-f1d6fc5116004de9b68c5f6380bbb4e5
出典データセット
uspto-grants-1984_12
特許番号
US04486444

反応ノート

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