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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-bromo-2-hydroxy-6-methylbenzoate | HCID 66685369 | — |
| Solvent | methyl 7-(benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-carboxylate | HCID 66685555 | — |
| Product | Methyl 3-bromo-2-methoxy-6-methylbenzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266896B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-c712cf0b68ac444d868d42e229916df0 |
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| Source note | uspto-grants-2016_02 |
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