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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094871Generated: October 30, 2026

Sodium Methoxide → 7-Methoxy-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid

https://huagongshe.com/reaction/2094871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 7-bromo-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylateHCID 52107335—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-Methoxy-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acidHCID 5742233157%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445692B2
Source datasetuspto-grants-2013_05
ORD IDord-2bb04b08c0f24f24ac9d794b1696688f
Source noteuspto-grants-2013_05