HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604648Generated: October 31, 2026
Dimethylformamide → Methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate
https://huagongshe.com/reaction/1604648
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Tert-butylthiazol-2-yl)benzofuran-5-yl trifluoromethanesulfonate | HCID 19603684 | — |
| Reactant | 1,3-Bis(diphenylphosphono)propane | HCID 53851155 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate | HCID 19603836 | — |
Reaction Steps
Carbon monoxide was introduced by bubbling to a mixture of 2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl trifluoromethanesulfonate (6.0 g), palladium acetate (99.7 mg), 1,3-bis(diphenylphosphono)propane (183 mg, 0.44 mmol) and triethylamine (4.13 ml) in a mixed solvent of methanol (15 ml) and N,N-dimethylformamide (30 ml) at room temperature for 1 hour. The mixture was warmed to 70° C. and stirred under carbon monoxide balloon for 3 hours. The resulting mixture was filtered through celite and the residue was washed with ethyl acetate. The filtrate and washing solution was combined and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using ethyl acetate-n-hexane as eluent to give methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate (3.92 g) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994378 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-438352edabd341d88dfbc1795d420f22 |
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| Source note | uspto-grants-1999_11 |
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