HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022385Generated: October 30, 2026
Sulfuric Acid → (5-Bromo-4-fluoro-2-methyl-phenyl)-acetic acid methyl ester
https://huagongshe.com/reaction/1022385
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-Bromo-2-fluoro-4-methyl-5-(2,2,2-trichloro-ethyl)-benzene | HCID 59614589 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-Bromo-4-fluoro-2-methyl-phenyl)-acetic acid methyl ester | HCID 59614585 | — |
Reaction Steps
To a solution of 1-bromo-2-fluoro-4-methyl-5-(2,2,2-trichloro-ethyl)-benzene (29.2 g) in methanol (100 ml) is added a sodium methoxide solution (30% in methanol, 78.2 ml) dropwise. The reaction mixture is stirred at reflux for 24 hours, cooled to 5° C. and treated with concentrated sulfuric acid (13.2 ml) dropwise. After further warming to reflux for 21 hours, the mixture is concentrated and the residue diluted with water/ethyl acetate. The aqueous layer is extracted with ethyl acetate, the combined organic layers are washed with brine, dried over sodium sulfate and concentrated. The residue is purified by chromatography on silica gel (ethyl acetate/cyclohexane 1:3). Yield: 18.76 g of (5-bromo-4-fluoro-2-methyl-phenyl)-acetic acid methyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722578B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-6381524a03d04d08a6ce5d06a44d1b80 |
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| Source note | uspto-grants-2014_05 |
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