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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460765Generated: October 29, 2026

Ethanol → HCID 15462098, compound

https://huagongshe.com/reaction/460765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium thiocyanateHCID 516872—
Reactant2-Bromo-4-chloro-1-(4-fluorophenyl)butan-1-oneHCID 3016587—
SolventWaterHCID 962—
ProductHCID 15462098HCID 15462098—

Reaction Steps

The 4-p-fluorophenyl-5-β-chloroethyl-4-thiazolin-2-one is prepared in the following manner: A mixture of 30 g of 1-p-fluorobenzoyl-1-bromo-3-chloropropane (prepared in accordance with our Italian Patent Application No. 23444 A/72 filed 22.4.1972), 11.5 g of potassium thiocyanate, 120 cc of ethanol and 6 cc of water is boiled under reflux for 4 hours. The precipitated solid is filtered while hot and 1-p-fluorobenzoyl-1-thiocyano-3-chloropropane precipitates from the filtrate on cooling. 22.1 g of the latter, 66 cc of glacial acetic acid and 11 cc of concentrated H2SO4 are boiled under relux for 4 hours. The acetic acid is removed from the reacting mass under reduced pressure and the residue is extracted while hot with chloroform. The chloroform solution is evaporated to dryness under reduced pressure and the residue recrystallised. M.P. = 138° C (from isopropyl alcohol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04061637
Source datasetuspto-grants-1977_12
ORD IDord-40744703f82e456f9aea27aaa3296dbb
Source noteuspto-grants-1977_12