HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538621Generated: October 28, 2026
Bromomethyl 3-methoxyphenyl ketone → 4-(3-Methoxyphenyl)-2-methyl-1,3-thiazole
https://huagongshe.com/reaction/538621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethyl 3-methoxyphenyl ketone | HCID 101294 | — |
| Reactant | Thioacetamide | HCID 2723949 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(3-Methoxyphenyl)-2-methyl-1,3-thiazole | HCID 19240283 | 83% |
Reaction Steps
A mixture of thioacetamide (8.0 g, 106.0 mmol) and 2-bromo-1-(3-methoxy-phenyl)-ethanone (2.0 g, 8.81 mmol) was heated at 140° C. for 6 h under nitrogen atmosphere. After completion of the reaction mixture (TLC monitoring), water (50 mL) was added and extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (230-400 M, 2% EtOAc-Hexane) to get the desired product (1.5 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865736B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f7cdb90aa4ed494686cb82b2e3a88876 |
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| Source note | uspto-grants-2014_10 |
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