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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597098Generated: October 31, 2026

Acetone → Methyl 4-[4-(2-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/1597098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethoxyphenacylbromideHCID 15556716—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylateHCID 86583815—
ProductMethyl 4-[4-(2-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylateHCID 8675742195%

Reaction Steps

Methyl 4-[4-(2-methoxyphenyl)(1,3-thiazol-2-yl)-5-methylthiothiophene-2-carboxylate: 105 mg (0.424 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge Chemical Co. LTD., Cornwall, U.K.) was dissolved in 5 mL of reagent grade acetone. 2-Bromo-2-methoxy acetophenone (0.467 mmol; 110 mg) was added and the solution was allowed to reflux for 3 h. The solution was allowed to cool and the solution concentrated. The crude product was dissolved in 100 mL of CH2Cl2 and washed one time with 50 mL of 1N NaOH. The organic layer was obtained, dried over sodium sulfate, concentrated and purified on a 1 mm silica plate eluting with 20% ethyl acetate/hexane to afford 160 mg (95% yield) of methyl 4-[4-(2-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-8da7372df40840fa97f913c4938db763
Source noteuspto-grants-2001_09