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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076833Generated: October 27, 2026

Ammonia → 1-(2-(4-Isothiocyanatophenoxy)ethyl)pyrrolidine

https://huagongshe.com/reaction/1076833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantCarbon DisulfideHCID 6348—
Reactant4-(2-(Pyrrolidin-1-yl)ethoxy)anilineHCID 6493749—
SolventEthanolHCID 702—
Product1-(2-(4-Isothiocyanatophenoxy)ethyl)pyrrolidineHCID 11846122—

Reaction Steps

4-(2-Pyrrolidin-1-ylethoxy)aniline (17.3 g.) in ethanol (20 ml.) is added dropwise to a mixture of ethanol (55 ml.), carbon disulphide (10 ml.) and aqueous ammonia (density = 0.88, 20 ml.) at 0°C. After 2 hours the solid is collected and washed with acetone, m.p. 143° - 150°C. (dec.). This solid (23.6 g.), chloroform (114 ml.) and triethylamine (11.9 ml.) are stirred, and ethyl chloroformate (8.6 ml.) added with cooling so that the temperature remains below 0°C. After stirring for 30 minutes below 0°C. and 1 hour at 20°C., excess of 10% sodium hydroxide is added. The chloroform is separated, washed with water, dried and evaporated. The residue is dissolved in benzene and the solution filtered through alumina. The filtrate is evaporated and the residue distilled to give 4-(2-pyrrolidin-1-ylethoxy)phenyl isothiocyanate, b.p. 160° - 168°C./0.2 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957999
Source datasetuspto-grants-1976_05
ORD IDord-e71717069173479e983c7ee1f0aaef0f
Source noteuspto-grants-1976_05