HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412957Generated: October 26, 2026
Bromomethyl 2-methoxyphenyl ketone → Methyl 4-[4-(2-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate
https://huagongshe.com/reaction/412957
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromomethyl 2-methoxyphenyl ketone | HCID 123440 | — |
| Reactant | Methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate | HCID 86583815 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 4-[4-(2-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate | HCID 86757421 | 104.4% |
Reaction Steps
Methyl 4-[4-(2-Methoxyphenyl)(1,3-thiazol-2-yl)]-5-metmylthiothiophene-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562840B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-04be389e5635427692f6116ed9ed15ea |
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| Source note | uspto-grants-2003_05 |
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