HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900579Generated: October 31, 2026
Lithium Hydroxide → 4-Acetamido-5-chloro-2-methoxybenzoic acid
https://huagongshe.com/reaction/900579
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 4-acetamido-5-chloro-2-methoxybenzoate | HCID 77721 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Acetamido-5-chloro-2-methoxybenzoic acid | HCID 10988496 | 50% |
Reaction Steps
4-Acetylamino-5-chloro-2-methoxy-benzoic acid methyl ester (2.09 g, 8.11 mmol) was dissolved in MeOH (110 ml) and LiOH solution (25.48 mmol in 30 ml, 1:1 MeOH:H2O) added and the solution stirred at room temperature for 6 hours. The solvent was concentrated in vacuo, EtOAc added and the organic phase was washed with 0.5N HCl then extracted with saturated NaHCO3 (2×). The aqueous phase was acidified with 12N HCl to pH 1 and the resulting precipitate extracted into CH2Cl2. The combined extracts were dried over anhydrous Na2SO4, filtered and evaporated to give the title compound as a white solid (0.933 g, 50% yield). 1H-NMR (500 MHz, CDCl3). δ 2.31 (s, 3H), 4.10 (s, 3H), 7.78-7.92 (br s, 1H), 8.17 (s, 1H), 8.45 (s, 1H). Analytical HPLC 5.62 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358273B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-588d498741a94a469dc2f41927a6700f |
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| Source note | uspto-grants-2008_04 |
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