HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11651Generated: October 30, 2026
2-(5-Chloro-2-methoxyphenyl)acetic acid → 2-(5-Chloro-2-hydroxyphenyl)acetic acid
https://huagongshe.com/reaction/11651
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(5-Chloro-2-methoxyphenyl)acetic acid | HCID 1504047 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(5-Chloro-2-hydroxyphenyl)acetic acid | HCID 244199 | 88.5% |
Reaction Steps
A solution of (5-chloro-2-methoxy-phenyl)-acetic acid (15.5 g, 77.5 mmol) in 48% aqueous hydrogen bromide was heated to reflux for 20 hours. The solution was cooled, diluted with water and extracted with diethyl ether. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The crude product was purified by trituration in 2:1 methylene chloride:hexanes to give (5-chloro-2-hydroxy-phenyl)-acetic acid (12.8 g). This was dissolved in a solution of ethanol saturated with hydrochloric acid and stirred 12 hours. The reaction was concentrated in vacuo, then the crude product was dissolved in diethyl ether and washed with saturated aqueous sodium hydrogen carbonate. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo to give the title compound (12.7 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098212B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-6964a5abe9d54700b29d9f3cdfe61c87 |
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| Source note | uspto-grants-2006_08 |
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