2-Chloroethanesulfinic chloride → Phenyl 2-chloroethanesulfinate
反応式
[O-:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Tl+].[Cl:9][CH2:10][CH2:11][S:12](Cl)=[O:13]>CCOCC>[Cl:9][CH2:10][CH2:11][S:12]([O:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:13]参加物
4
実験手順
A suspension of thallium (I) phenoxide (28.6 w) in dry ether (100 v) was rapidly treated with 2-chloroethanesulfinyl chloride, prepared as in Example I. The slurry was vigorously stirred for 1 hour at ambient temperature with exclusion of moisture. Removal of thallium(I) chloride by filtration and evaporation of the etheral filtrate solution gave an oil. The oil was then subjected to molecular distillation in a wiped-film apparatus at 70-75° (1 ×10-4 torr) to give phenyl 2-chloroethanesulfinate (122 w) as a mobile liquid.
後処理
- customRemoval of thallium(I) chloride
- filtrationby filtration and evaporation of the etheral filtrate solution
- customgave an oil
- distillationThe oil was then subjected to molecular distillation in a wiped-film apparatus at 70-75° (1 ×10-4 torr)
出典と根拠
- ORDレコード
- ord-c940ef5caa644eafbafa74fff11d2d54
- 出典データセット
- uspto-grants-1979_01
- 特許番号
- US04134752
反応ノート
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