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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103807Generated: October 29, 2026

Hydrogen Bromide → 3-Bromo-4-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/2103807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantEthyl AcetateHCID 8857—
Reactant3-Amino-4-(methoxycarbonyl)benzoic acidHCID 5235500—
ReactantSodium NitriteHCID 23668193—
CatalystCupric ChlorideHCID 24014—
SolventAcetic AcidHCID 176—
Product3-Bromo-4-(methoxycarbonyl)benzoic acidHCID 1867302659%

Reaction Steps

To 3-amino-4-methoxycarbonylbenzoic acid (1.95 g, 10 mmol) suspended in 48% hydrobromic acid (50 mL) and acetic acid (50 mL), an aqueous solution (20 mL) of sodium nitrite (0.69 g, 10 mmol) was added at −10° C., and the resulting solution was stirred for 30 minutes. The solution was added to copper bromide (I) (1.44 g, 10 mmol) in 48% hydrobromic acid (50 mL) at −10° C., and the resulting reaction mixture was stirred at room temperature for 1 hour. After addition of ethyl acetate, the reaction mixture was washed with water, dried over magnesium sulfate, filtered through celite and purified by silica gel column chromatography to give 1.70 g of the desired product as a colorless solid (yield 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576115B2
Source datasetuspto-grants-2009_08
ORD IDord-e8c90d15314c4686a395f22a19bf4e75
Source noteuspto-grants-2009_08