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HRID 370556作成日:2026年10月25日

Butyl-p-toluenesulfonate → Hydrochloric Acid

https://huagongshe.com/reaction/370556

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl-p-toluenesulfonateHCID 13066—
反応物Sodium hydrideHCID 24758—
反応物(R)-2-(2,4-dichlorophenyl)-1-(imidazol-1-yl)-3-mercapto-2-propanolHCID 13420610—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Hydrochloric AcidHCID 3131,386%
生成物(R)-3-(n-butylthio)-2-(2,4-dichlorophenyl)-1-(imidazol-1-yl)-2-propanolHCID 13420611—

反応手順

To a solution of (R)-2-(2,4-dichlorophenyl)-1-(imidazol-1-yl)-3-mercapto-2-propanol (II) (3 g) in dry N,N-dimethylformamide (20 ml) were added a 50% dispersion of sodium hydride in paraffin (1 g) and n-butyl p-toluenesulfonate (2.3 g) at 0°-5° C. in nitrogen atmosphere. The mixture was stirred at 0°-5° C. for 1 hour and at 20°-25° C. for 18 hours. The reaction mixture was diluted with water (200 ml) and extracted with dichloromethane. Treatment of the extract in the same manner as in Example 4 gave (R)-3-(n-butylthio)-2-(2,4-dichlorophenyl)-1-(imidazol-1-yl)-2-propanol (I: n=3) hydrochloride (2.5 g). Yield, 63.8%. M.P., 168°-169° C. [α]D20 -88.8° (c=1, methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04526983
出典データセットuspto-grants-1985_07
ORD IDord-5de86fa94cf0496f835b0e09c317dae8
出典メモuspto-grants-1985_07