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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716955Generated: November 1, 2026

Water → 5-Bromo-2-chloro-4-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/1716955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-ButanolHCID 6386—
Reactant18-Crown-6HCID 28557—
Reactant2-Bromo-5-chloro-4-methyl-benzoic acid methyl esterHCID 53330616—
Product5-Bromo-2-chloro-4-(methoxycarbonyl)benzoic acidHCID 45480503—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of methyl 2-bromo-5-chloro-4-methylbenzoate (39.53 g, 0.15 mol), 18-Crown-6 (3.95 g), tert-butyl alcohol (350 mL), and water (750 mL) was combined together with mechanical stirring. The reaction mixture was heated to reflux and monitored by TLC. After refluxing overnight, the reaction was cooled to 55° C. and filtered. The filter cake was washed with hot water (2×100 mL, 50° C.). The filtrate was neutralized with 18% hydrochloric acid to pH 1 and stored in refrigerator (0˜5° C.) for 3 h. It was filtered, washed with ice water (2×50 mL) and petroleum ether (2×50 mL). The filter cake was dried under vacuum to give the title compound as a white crystalline. Yield: 32.1 g (73%). 1H NMR (DMSO-d6, 300 MHz): δ 8.10 (s, 1H), 7.89 (s, 1H), 3.86 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803778B2
Source datasetuspto-grants-2010_09
ORD IDord-5c12185339984e0c81e382300fb1c918
Source noteuspto-grants-2010_09