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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298630Generated: October 26, 2026

Phenacyl bromide → Methyl 5-methyl-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxylate

https://huagongshe.com/reaction/2298630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiophene-2-carboxylateHCID 18537096—
ProductMethyl 5-methyl-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxylateHCID 18536825—

Reaction Steps

A solution of 200 mg (0.93 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiophene-2-carboxylate was reacted with 185 mg (0.93 mmol) of 2-bromoacetophenone in a manner similar to Example 8, step (a) to give, after purification by preparative thin layer chromatography eluting with hexanes:ethyl acetate 7/3 (v:v), a mixture of methyl 5-methyl-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxylate and methyl 4-cyano-5-methylthiophene-2-carboxylate (96 mg, 36%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-0b3daf0446e8408ba5b94533e4ab34a1
Source noteuspto-grants-2002_12