Ethyl benzoate → Ethyl thiobenzoate
反応式
[C:1]([O:9][CH2:10][CH3:11])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:21])=CC=1>C1(C)C(C)=CC=CC=1.CCCCCC>[C:1]([O:9][CH2:10][CH3:11])(=[S:21])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
5
実験手順
70 ml (0.487 mol) of ethyl benzoate were heated to reflux for 12 hours with 100 g (0.247 mol) of Lawesson reagent in 350 ml of xylene. After cooling to 20° the reaction mixture was diluted with 500 ml of hexane and filtered. The filtrate was flash-chromatographed on 1 kg of silica gel. Elution was carried out with hexane. The fractions which were pure according to the thin-layer chromatogram (eluent: toluene) were combined and evaporated under reduced pressure. There were obtained 72 g (89%) of O-ethyl thiobenzoate as a dark yellow evil-smelling oil which was used without further purification.
後処理
- temperatureAfter cooling to 20° the reaction mixture
- filtrationfiltered
- customThe filtrate was flash-chromatographed on 1 kg of silica gel
- washElution
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-b9fb0c3db8d740fd9947a6d7688fb072
- 出典データセット
- uspto-grants-1993_04
- 特許番号
- US05204482
反応ノート
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