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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352039Generated: October 27, 2026

Lithium hydroxide, monohydrate → 2-Bromo-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoic acid

https://huagongshe.com/reaction/1352039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant2-Bromo-4-[[(3-hydroxybenzyl)amino]carbonyl]benzoic acid methyl esterHCID 23560771—
SolventWaterHCID 962—
SolventMeOH tetrahydrofuranHCID 21899815—
Product2-Bromo-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoic acidHCID 22661323102.7%

Reaction Steps

A solution of lithium hydroxide monohydrate (4.41 g, 105.1 mmol) in water (15 mL) was added to a solution of 2-bromo-4-[[[(3-hydroxyphenyl)methyl]amino]-carbonyl]benzoic acid, methyl ester (Example 14; 15.30 g, 42.0 mmol) in tetrahydrofuran/methanol (2:1, 21 mL). The solution was stirred at room temperature for 1 h, then it was concentrated to remove tetrahydrofuran and methanol. The remaining aqueous solution was extracted with ethyl acetate (15 mL) and the ethyl acetate extract was discarded. The aqueous layer was acidified with 1 M HCl (75 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine (15 mL), dried (MgSO4), filtered, and evaporated to give 2-bromo-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoic acid (15.1 g, quantitative yield) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217728B2
Source datasetuspto-grants-2007_05
ORD IDord-15aaf82e16a34c46a6c1af4a1be0dc93
Source noteuspto-grants-2007_05