反応式
[C:1]([SH:9])(=[S:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:10]([O:13][CH:14]=[CH2:15])(=[O:12])[CH3:11]>C(Cl)(Cl)(Cl)Cl>[C:1]([S:9][CH:14]([O:13][C:10](=[O:12])[CH3:11])[CH3:15])(=[S:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
反応条件
- 温度
- 70 °C
実験手順
A mixture of dithiobenzoic acid (4 g), vinyl acetate (10 mL) and carbon tetrachloride (15 mL) was heated at 70° C. for 16 hours. The resultant mixture was reduced and the residue purified by column chromatography (aluminium oxide column (activity III), n-hexane eluent) to give 1-acetoxyethyl dithiobenzoate (6) (3.21 g, 51.5% yield) as a dark red oil. 1H-nmr (CDCl3) d (ppm): 1.80 (d, 3H); 2.09 (s, 3H); 6.75 (q, 1H); 7.34-7.60 (m, 3H) and 7.97 (m, 2H).
後処理
- customthe residue purified by column chromatography (aluminium oxide column (activity III), n-hexane eluent)
出典と根拠
- ORDレコード
- ord-b7cd406a74e549b695a4ade2e0bb10bf
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07714075B1
関連ノート
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