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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660158Generated: October 31, 2026

Water → 1-(2-Furfuryl)-2-thiourea

https://huagongshe.com/reaction/1660158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium thiocyanateHCID 15666—
ReactantHCID 11457720HCID 11457720—
SolventBromobenzeneHCID 7961—
Product1-(2-Furfuryl)-2-thioureaHCID 71769930.9%

Reaction Steps

Furfurylamine hydrochloride (33.46 grams, 0.250 moles) and ammonium thiocyanate (38.14 grams, 0.501 moles) in 71 ml bromobenzene were heated under nitrogen at reflux temperature for 20 minutes and then cooled to room temperature. The reaction mixture was mixed with a solution of 125 ml water and 100 ml ethyl acetate and left at room temperature overnight. The mixture was then diluted to give 500 ml ethyl acetate and 350 ml water and the aqueous layer separated. The organic layer was washed with water and dried over sodium sulfate. After filtration, the organic layer was evaporated to dryness and bromobenzene removed under vacuum. The resulting solids were ground in a mortar and pestle and the fine particles stirred in diethyl ether to remove residual bromobenzene. The solids were then filtered, washed with diethyl ether and vacuum dried over phosphorus pentoxide, yielding 12.06 grams (30%) of N-furfurylthiourea, m.p. 80°-91° C. Recrystallization from benzene gave yellow needles, m.p. 98°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307106
Source datasetuspto-grants-1981_12
ORD IDord-014813ae75574d57810d2e24129fe08b
Source noteuspto-grants-1981_12