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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725882Generated: November 1, 2026

Water → 3-Bromo-6-{[(tert-butoxy)carbonyl]amino}-2-methylbenzoic acid

https://huagongshe.com/reaction/1725882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-((tert-Butoxycarbonyl)amino)-6-methylbenzoic acidHCID 22245123—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventDimethylformamideHCID 6228—
Product3-Bromo-6-{[(tert-butoxy)carbonyl]amino}-2-methylbenzoic acidHCID 6886644788.6%

Reaction Steps

A solution of Example 104A (10 g, 40 mmol) and tetrabutylammonium tribromide (19.2 g, 40 mmol) in DMF (250 mL) was treated slowly with water (250 mL). The resulting suspension was stirred for 18 hours and partitioned between water (1.2 L) and ethyl acetate (500 mL). The organic layer was washed with water (2×1 L), dried (Na2SO4), filtered, and concentrated. The residue was dissolved in dichloromethane (900 mL), washed with water (5×1 L) and brine, dried (Na2SO4), filtered, and concentrated to provide the desired product (11.7 g). MS (ESI(−)) m/e 328, 330 (M−H)−; 1H NMR (300 MHz, DMSO-d6) δ 13.60 (br s, 1H), 9.68 (s, 1H), 7.63 (d, 1H), 7.39 (d, 1H), 2.37 (s, 3H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491718B2
Source datasetuspto-grants-2009_02
ORD IDord-184c9bdfbf784ffe92c977493bde5054
Source noteuspto-grants-2009_02