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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286338Generated: October 31, 2026

Phenacyl bromide → HCID 23463072, compound

https://huagongshe.com/reaction/2286338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant2-Chlorobenzoyl chlorideHCID 69110—
Reactant5-(2-Chlorophenyl)-1,3,4-thiadiazol-2-amineHCID 554211—
ReactantThiosemicarbazideHCID 2723789—
SolventDimethylformamideHCID 6228—
ProductHCID 23463072HCID 23463072—

Reaction Steps

10.5 g (0.05 mol) of 2-amino-5-(2-chlorophenyl)-1,3,4-thiadiazole, melting point 189,5° C. (prepared by reacting thiosemicarbazide with 2-chlorobenzoyl chloride) together with 10 g (0.05 mol) of bromoacetophenone are warmed to 120° C. in 100 ml of dimethylformamide for 3 hours and the mixture is then cooled and concentrated in a rotary evaporator. After digesting the residue with water, the digestion mixture is filtered and the residue is recrystallised from alcohol. A second fraction is obtained by concentrating the alcoholic mother liquor. A total yield of 12.5 g, corresponding to 80% of theory, of colourless crystals of melting point 126° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04265898
Source datasetuspto-grants-1981_05
ORD IDord-9f593c31b76e42e983b3e5a8b3cec8a0
Source noteuspto-grants-1981_05