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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778367Generated: October 30, 2026

Dimethyl Sulfate → Methyl 3-bromo-2-methoxy-6-methylbenzoate

https://huagongshe.com/reaction/1778367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-bromo-2-hydroxy-6-methylbenzoateHCID 66685369—
Solventmethyl 7-(benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-carboxylateHCID 66685555—
ProductMethyl 3-bromo-2-methoxy-6-methylbenzoateHCID 66685292—

Reaction Steps

A mixture of methyl 3-bromo-2-hydroxy-6-methylbenzoate (Intermediate 44, 114.5 g), dimethyl sulfate (61 mL) and potassium carbonate (166 g) in acetone (11) was heated at reflux for 2.5 hours. After cooling, the mixture was filtered and the filtrate was evaporated to dryness. The residue was dissolved in DCM and washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of tert-butyl methyl ether and pentane with a gradient of 0-40%. The product was purified again by chromatography on silica, eluting with a mixture of tert-butyl methyl ether and pentane with a gradient of 0-10%. The product was again purified by chromatography on silica, eluting with a mixture of tert-butyl methyl ether and pentane with a gradient of 0-10% to give methyl 3-bromo-2-methoxy-6-methylbenzoate (66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266896B2
Source datasetuspto-grants-2016_02
ORD IDord-c712cf0b68ac444d868d42e229916df0
Source noteuspto-grants-2016_02