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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597096Generated: October 26, 2026

Bromomethyl 3-methoxyphenyl ketone → HCID 86583812, compound

https://huagongshe.com/reaction/1597096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 3-methoxyphenyl ketoneHCID 101294—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylateHCID 86583815—
SolventAcetoneHCID 180—
ProductHCID 86583812HCID 8658381264.5%

Reaction Steps

Methyl 4-[4-(3-methoxyphenyl)(1,3-thiazol-2-yl)-5-methylthiothiophene-2-carboxylate: 32 mg (0.133 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge Chemical Co. LTD., Cornwall, U.K.) was dissolved in 2 mL of reagent grade acetone. 3′-Methoxy-2-bromo acetophenone (0.155 mmol; 36 mg; Aldrich Chemical Co.) was added and the solution was allowed to reflux for 2.5 h. The solution was allowed to cool and a solid was filtered and washed with methanol and dried in vacuo. The solid was purified on 1 mm silica plate eluting with 25% ethyl acetate/hexane to afford 31 mg (63% yield) of methyl 4-[4-(3-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291514B1
Source datasetuspto-grants-2001_09
ORD IDord-70722cd983354e4c9a577eb69ee991c1
Source noteuspto-grants-2001_09