反応式
[CH3:1][C:2]1[CH:3]=[C:4]([C:7]([OH:9])=O)[S:5][CH:6]=1.S(Cl)([Cl:12])=O>>[CH3:1][C:2]1[CH:3]=[C:4]([C:7]([Cl:12])=[O:9])[S:5][CH:6]=1参加物
3
実験手順
220 cc of thionyl chloride were progressively added to 50 gm of 4-methyl-thiophene-2-carboxylic acid [prepared by process in Beil, Vol. 18, p. 294] and the mixture was heated to reflux for 1 hour. Excess thionyl chloride was evaporated off under reduced pressure and the residue was distilled under reduced pressure to obtain 51 gm of 4-methyl-thiophene-2-carboxylic acid chloride boiling at 112°-114° C. at 18 mm Hg. which was used as is for the next step. The light yellow liquid was soluble in ether.
後処理
- temperaturethe mixture was heated
- temperatureto reflux for 1 hour
- customExcess thionyl chloride was evaporated off under reduced pressure
- distillationthe residue was distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-c493992beac446d09e5a65cf124daa83
- 出典データセット
- uspto-grants-1979_07
- 特許番号
- US04159986
関連ノート
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