HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051238Generated: October 31, 2026
HCID 15735723, compound → 2-[[2-Chloro-3-(1-hydroxyethyl)phenyl]amino]benzoic acid
https://huagongshe.com/reaction/2051238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15735723 | HCID 15735723 | — |
| Reactant | (2-Carboxyphenyl)phenyliodonium hydrate (1:1) | HCID 22271963 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-[[2-Chloro-3-(1-hydroxyethyl)phenyl]amino]benzoic acid | HCID 15735724 | 65.6% |
Reaction Steps
A mixture of diphenyliodonium-2-carboxylate monohydrate (11.4 g, 33.3 mmol), 3-amino-2-chloro-α-methylbenzenemethanol (5.2 g, 30.3 mmol), and cupric acetate (0.5 g) in isopropanol (100 mL) is heated at reflux for 12 hours under an argon atmosphere. The solvent is evaporated under vacuum and the remaining dark oil is taken up in 10% aqueous KOH. The insoluble material is removed by filtration through Celite-545, and the filtrate is extracted with ether to remove nonacidic impurities. The aqueous solution is acidified to pH=3 with concentrated HCl. The resulting precipitate is collected by filtration and purified by column chromatography (silica, ethyl acetate) to give pure 2-[[2-chloro-3-(1-hydroxyethyl)phenylamino]benzoic acid (5.8 g, 60%), mp=169-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05017604 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-028b15ebcf4b4d1581ee51324ff8a9f9 |
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| Source note | uspto-grants-1991_05 |
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