Acetone → 1-((Trifluoromethyl)thio)-2-propanone
反応式
[CH3:1][C:2](=[O:4])[CH3:3].C(O)C.[F:8][C:9]([F:13])([F:12])[S:10]Cl>ClCCl>[F:8][C:9]([F:13])([F:12])[S:10][CH2:1][C:2](=[O:4])[CH3:3]参加物
反応条件
- 温度
- 25 °C
実験手順
A mixture of 2-propanone (0.25 mole), ethanol (0.49) and dichloromethane (75 ml) was introduced into a sealed and pressure tested vessel having a volume of about 500 ml under reduced pressure. Trifluoromethanesulfenyl chloride (0.22 mole) was then added to the cooled, evacuated vessel. The vessel was warmed to about 25°C and then rocked for five days. The vessel was vented through a cold gas trap (-78°C) to trap any unreacted trifluoromethylsulfenyl chloride gas and then through a scrubbing system to remove the vented hydrogen chloride gas. Residual liquid was transferred to a flask and distilled to give about 24 g of 1-trifluoromethylthio-2-propanone. The structure of the purified product (b.p. 51°-52°C/22 mm Hg) was confirmed by spectral and elemental analyses.
後処理
- additionwas introduced into
- customa sealed
- customevacuated vessel
- customThe vessel was vented through a cold gas trap
- custom(-78°C) to trap any unreacted trifluoromethylsulfenyl chloride gas and then through a scrubbing system to remove the vented hydrogen chloride gas
- customResidual liquid was transferred to a flask
- distillationdistilled
出典と根拠
- ORDレコード
- ord-25ba989268a746fcb747b690c8fdbfa4
- 出典データセット
- uspto-grants-1976_02
- 特許番号
- US03937738
反応ノート
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