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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492394Generated: October 31, 2026

Hydrogen Bromide → Benzoic acid, 3-bromo-4-chloro-2-methyl-, ethyl ester

https://huagongshe.com/reaction/1492394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 18950361HCID 18950361—
ReactantSodium NitriteHCID 23668193—
Catalystcopper(I) bromideHCID 24593—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductBenzoic acid, 3-bromo-4-chloro-2-methyl-, ethyl esterHCID 18950362—

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of sodium nitrite (13 g) in concentrated sulphuric acid was added during 0.5 hours to a solution of ethyl 3-amino-4-chloro-2-methylbenzoate (22.4 g) in acetic acid, keeping the temperature below 15° C. After stirring for a further 1 hour at 5° C., the resulting diazonium mixture was added during 0.75 hours to a solution of copper (I) bromide (31 g) in hydrobromic acid (45%, 103 ml) and water. Heating to 40° C. was continued for a further 2 hours before addition of water and extraction (ethyl acetate). The extract was washed (sodium hydroxide solution), dried (magnesium sulphate) and evaporated to give ethyl 3-bromo-4-chloro-2-methylbenzoate (22.2 g) as a brown oil, NMR (CDCl3) 1.3 (t,3H), 2.65 (s,3H), 4.3 (q,2H), 7.45 (m,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374606
Source datasetuspto-grants-1994_12
ORD IDord-679e892a7e9e4c22a0a62553ebfc1439
Source noteuspto-grants-1994_12