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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47273Generated: October 25, 2026

Carbon Disulfide → 2-(2-Isothiocyanatoethyl)-1-methylpyrrolidine

https://huagongshe.com/reaction/47273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantEthyl chloroformateHCID 10928—
Reactant2-(2-Aminoethyl)-1-methylpyrrolidineHCID 98388—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product2-(2-Isothiocyanatoethyl)-1-methylpyrrolidineHCID 2199232843.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of carbon disulfide (0.996 mL, 16.57 mmol) in water (5 mL) was cooled to 0° C. Then 2-(2-aminoethyl)-1-methylpyrrolidine (2.4 mL, 16.57 mmol) was added over 45 minutes. The resulting mixture was maintained at 0° C. for an additional 30 minutes and then the cooling was discontinued. Next, ethyl chloroformate (1.58 mL, 16.57 mmol) was added over a 1 h period. The resulting mixture was maintained at room temperature for an additional 30 minutes and then made basic with saturated sodium hydrogen carbonate in water. The mixture was extracted with diethyl ether (2×50 mL). The extracts were combined, washed with brine (15 mL), dried over anhydrous sodium sulfate, filtered, and concentrated to give a pale yellow oil. The oil was purified by vacuum distillation to give 1.22 g of 2-(2-isothiocyanatoethyl)-1-methylpyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699866B2
Source datasetuspto-grants-2004_03
ORD IDord-a3386d6f29e44d2a8fa2b0fb1a07ae9a
Source noteuspto-grants-2004_03