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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285384Generated: October 31, 2026

Phenacyl bromide → HCID 13476634, compound

https://huagongshe.com/reaction/1285384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 5-acetamido-4-cyano-3-methylthenoateHCID 90296—
SolventAcetoneHCID 180—
ProductHCID 13476634HCID 1347663480.4%

Reaction Steps

250 g of 2-acetamido-3-cyano-4-methyl-5-ethoxycarbonylthiophene, prepared in accordance with the method of K. Gewald, are refluxed for 24 hours in 1500 ml of acetone with 250 g of α-bromoacetophenone and 220 g of potassium carbonate; the whole is then precipitated in 4000 ml of ice-water. The resulting precipitate is filtered, washed with 1000 ml of an iced mixture of water/ethanol (1/1), then dried and finally washed with 1000 ml of a cold mixture of cyclohexane/benzene (9/1). In this manner 295 g of 2-ethoxycarbonyl-3-methyl-4-amino-5-benzoyl-6-acetylthieno[2,3-b]pyrrole are obtained, m.p.: 188° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567196
Source datasetuspto-grants-1986_01
ORD IDord-8777bd1be36243eca06368f1293ef212
Source noteuspto-grants-1986_01