HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646274Generated: October 29, 2026
Dimethyl Sulfate → Methyl 5-bromo-2-methoxybenzoate
https://huagongshe.com/reaction/646274
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 5-Bromosalicylic acid | HCID 6972 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 5-bromo-2-methoxybenzoate | HCID 13297188 | — |
Reaction Steps
5-Bromo-2-hydroxybenzoic acid (25 g) and 40 g of potassium carbonate were suspended in 300 mL of acetone. Dimethyl sulfate (28 mL) was added to the suspension, and the mixture was stirred for 19 hours under reflux with heating. The reaction mixture was cooled to room temperature, whereafter the insolubles were separated by filtration, and washed with ethyl acetate. The filtrate and the washings were combined, and acetone and ethyl acetate were distilled off under reduced pressure. The resulting residue was dissolved in 300 mL of ethyl acetate. Water (300 mL) was added to the solution, and the organic layer was separated; followed by extracting the aqueous layer with 200 mL of ethyl acetate. After the respective organic layers were combined, the combined organic layer was washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was separated by filtration, and then washed with ethyl acetate. The filtrate and the washings were combined, and ethyl acetate was distilled off under reduced pressure to obtain 30 g of methyl 5-bromo-2-methoxybenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705053B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d6d1a8834a9345d3a04b8c171dab07e1 |
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| Source note | uspto-grants-2010_04 |
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