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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350872Generated: October 30, 2026

Hydrochloric Acid → HCID 14500676, compound

https://huagongshe.com/reaction/2350872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-chloroacetoacetateHCID 11858—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(4-Chlorophenyl)-3-thiosemicarbazideHCID 706988—
SolventEthanolHCID 702—
ProductHCID 14500676HCID 1450067613.6%

Reaction Steps

A suspension of 20.1 g (0.10 mole) of 4-(4-chlorophenyl)3-thiosemicarbazide in 80 mL of absolute ethanol was treated with 16.5 g (0.10 mole) of ethyl 2-chloroacetoacetate and the mixture stirred for 1.0 hr at room temperature. Alcoholic hydrogen chloride (2N, 60 mL) was added and the dark precipitate dissolved while heating the mixture at reflux for 1.0 hr. The solution was filtered while hot, and the filter cake washed with absolute ethanol. The filtrate was evaporated under reduced pressure and the residue triturated in cold absolute ethanol and filtered. Both filter cakes were found to be the same compound by TLC (10% methanol in benzene on silica gel). The two were combined, dissolved in hot absolute ethanol (the hydrochloride salt was water insoluble), partially neutralized with saturated aqueous sodium bicarbonate, and the solid filtered (10.4 g, mp 212°-226° C.). A second crop was obtained by treating the filtrate with saturated aqueous sodium bicarbonate (11.5 g, mp 220°-225° C.). The second crop was recrystallized from absolute ethanol to give 3.8 g of product, mp 223°-225° C. This solid was dried at 100° C./0.1 mmHg/3 hr; then for ~16 hr at RT/0.1 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871737
Source datasetuspto-grants-1989_10
ORD IDord-a96b09f6351a42b38d6151e58b80431e
Source noteuspto-grants-1989_10