Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47280Generated: October 26, 2026

Chloride → 3-(Dimethylamino)pyrrolidine-1-carbothioamide

https://huagongshe.com/reaction/47280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantPotassium thiocyanateHCID 516872—
Reactant3-(Dimethylamino)pyrrolidineHCID 2758519—
SolventAcetoneHCID 180—
Product3-(Dimethylamino)pyrrolidine-1-carbothioamideHCID 2062803523.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of potassium thiocyanate (2.02 g, 20.8 mmol) in acetone (10.7 mL) at 0° C. was slowly added pivolyl chloride (2.6 mL, 21.1 mmol). The mixture was stirred at 0° C. for 3 h. Dimethylpyrrolidin-3-yl-amine (2.44 g, 21.3 mmol) was added slowly at 0° C., and the reaction was allowed to warm to room temperature. After stirring at room temperature overnight, the reaction was concentrated, and concentrated hydrochloric acid (10 mL) was added. The reaction was heated to 95° C. with stirring for 1 h. The mixture was allowed to cool to room temperature, and was extracted with dichloromethane. The aqueous layer was made basic with 20% aqueous sodium hydroxide. The basic solution was extracted with dichloromethane. The organics were combined, washed with brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The mixture was diluted with diethyl ether and filtered to provide pure 3-dimethylamino-pyrrolidine-1-carbothioic acid amide (135) (0.863 g, 23.3%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699866B2
Source datasetuspto-grants-2004_03
ORD IDord-55c08c4e2abf434b924357fc47dc6c8d
Source noteuspto-grants-2004_03