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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660159Generated: October 29, 2026

2-Bromopropiophenone → HCID 20558016, compound

https://huagongshe.com/reaction/1660159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropiophenoneHCID 16452—
Reactant1-(2-Furfuryl)-2-thioureaHCID 717699—
SolventEthanolHCID 702—
ProductHCID 20558016HCID 2055801633.3%

Reaction Steps

N-furfurylthiourea (0.82 grams, 0.005 moles) and α-bromopropiophenone (1.07 grams, 0.005 moles, Aldrich Chem. Co.) in 11 ml absolute ethanol were heated to reflux temperature under nitrogen for 3 hours. After cooling to room temperature, the solvent was removed under vacuum to give a thick brown oil, which was triturated with five 35 ml portions of refluxing ethyl acetate. The ethyl acetate was reduced in volume to about 25 ml and cooled to room temperature. The precipitated solids were filtered, washed with ethyl acetate and vacuum dried over phosphorous pentoxide, yielding 0.585 grams (33%) of 2-furfurylamino-5-methyl-4-phenyl-thiazole hydrobromide, m.p. 150°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307106
Source datasetuspto-grants-1981_12
ORD IDord-2fb5f3923dbe497787edbd608a630467
Source noteuspto-grants-1981_12