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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973627Generated: November 3, 2026

Ethanol → HCID 54306529, compound

https://huagongshe.com/reaction/1973627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-(Chloroacetyl)pyrrolidineHCID 88440—
ReactantPotassium thiocyanateHCID 516872—
SolventPentaneHCID 8003—
ProductHCID 54306529HCID 54306529—

Reaction Steps

1-(α-Chloroacetyl pyrrolidine (14.7 grams; 0.1 mol), potassium thiocyanate (18 grams; 0.2 mol) and ethanol (50 ml) were charged into a glass reaction flask equipped with a mechanical stirrer and reflux condenser. The reaction mixture was heated at reflux, with stirring, for a period of about 4 hours. The mixture was then cooled and filtered. The filtrate was stripped of solvent to yield a solid product. The solid was extracted with three 200 ml portions of boiling benzene, and the benzene extracts were combined and evaporated under reduced pressure to yield an oil. The oil was poured into pentane wherein it solidified. The solid was recrystallized from a benzene-pentane mixture to yield 1-(α-thiocyanoacetyl) pyrrolidine having a melting point of 95° to 96° C. and having the following elemental analysis; calculated for C7H10N2OS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998808
Source datasetuspto-grants-1976_12
ORD IDord-e2d520103c0348c1b979183eb8c229f6
Source noteuspto-grants-1976_12