反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5]Br.[C:10](O)(=O)[CH2:11][SH:12].[OH-:15].[K+]>C(O)C.O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][CH2:10][C:11]([OH:15])=[S:12])[CH:7]=[CH:8][CH:9]=1参加物
実験手順
To a solution of 3-bromobenzyl bromide (23.75 g, 90 mmol) and thioglycolic acid (11.42 g, 120 mmol) in ethanol (150 mL) was added potassium hydroxide (14.24 g, 250 mmol) in water (50 mL). The reaction was heated at reflux for 3.5 h, cooled and the ethanol was evaporated. The residue was quenched with water (100 mL) and the mixture was extracted with ether (50 mL). The aqueous layer was acidified to pH 1 with concentrated hydrochloric acid, extracted with ethyl acetate (2×100 mL) and the organic phase was dried. Evaporation of the solvent followed by washing of the residue with hexane afforded 3-bromophenylmethylthioacetic acid as a white solid (92%), mp 90°-91° C.: 1H NMR (CDCl3) δ3.10 (s, 2H), 3.82 (s, 2H), 7.20-7.29 (m, 2H), 7.39-7.42 (dd, 1H), 7.52 (d, 1H); IR (KBr) 1706 cm-1 ; Mass spectrum m/z 280 (M+NH4); Anal. calcd. for C9H9O2SBr: C 41.39, H 3.47, S 12.28; Found C 41.43, H 3.49, S 12.10.
後処理
- temperatureThe reaction was heated
- temperatureat reflux for 3.5 h
- temperaturecooled
- customthe ethanol was evaporated
- customThe residue was quenched with water (100 mL)
- extractionthe mixture was extracted with ether (50 mL)
- extractionextracted with ethyl acetate (2×100 mL)
- customthe organic phase was dried
- customEvaporation of the solvent
- washby washing of the residue with hexane
出典と根拠
- ORDレコード
- ord-cd69c48598cb494798ccebfd7e04088b
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05428040
関連ノート
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