HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988119Generated: November 2, 2026
Potassium → Methyl 7-(acetylamino)-1,3-benzodioxole-4-carboxylate
https://huagongshe.com/reaction/988119
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium | HCID 5462222 | — |
| Reactant | N-(7-iodo-1,3-benzodioxol-4-yl)acetamide | HCID 22662754 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 7-(acetylamino)-1,3-benzodioxole-4-carboxylate | HCID 22662748 | 128.6% |
Reaction Steps
A mixture of intermediate (2-b) (38.8 g), potassium acetae (20 g) and Pd/C (10%; 2 g) in CH3OH (500 ml) was stirred at 150° C. under 4.9×106 Pa (50 kg) pressure of CO, during 16 hours. The reaction mixture was cooled, filtered over dicalite, and the filtrate was evaporated. The residue was diluted with water, then extracted three times with DCM. The combined organic layers were dried, filtered and the solvent evaporated. The residue was dissolved in acetic acid (250 ml) and acetic anhydride (6 ml) was added dropwise. The mixture was stirred for 30 minutes at room temperature, then diluted with water (250 ml) and the resulting precipitate was filtered off, washed with water, then dried, yielding 19.4 g (64.7%) of methyl 7-(acetylamino)-1,3-benzodioxole-4-carboxylate (intermediate 2-c).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06635643B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-2ef6136ea09f4b4f864e8a3b4aa08877 |
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| Source note | uspto-grants-2003_10 |
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