HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548024Generated: October 28, 2026
Sodium Methoxide → 7-Methoxy-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid
https://huagongshe.com/reaction/548024
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 7-bromo-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate | HCID 52107335 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Methoxy-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid | HCID 57422331 | 57% |
Reaction Steps
In a 2 mL microwave vial, methyl 7-bromo-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate (273 mg, 1 mmol) and CuBr (14.3 mg, 0.1 mmol) were dissolved in dry DMF and was placed in ice bath. Sodium methoxide (540 mg, 10 mmol) was added into the reaction mixture dropwise while stirring at 0° C. The reaction was warmed to room temperature and stirred for 45 minutes. The reaction was then placed in a microwave reactor for 5 minutes at 135° C. The reaction mixture was dissolved in water and washed with ethyl acetate. The water layer was collected and acidified to pH 4 with 1M HCl. The product was extracted using ethyl acetate then dried over sodium sulfate. The solvent was evaporated under vacuum to give the desired intermediate of 7-methoxy-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid which was used directly without further purification. Yield 57%. MS M+H calculated 211.1, found 211.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07939671B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-c4a2e191823b4d31b7776061201c3f39 |
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| Source note | uspto-grants-2011_05 |
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