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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729387Generated: October 25, 2026

Acetic Acid → 2-Cyclopropylamino-4,5-difluorobenzoic acid

https://huagongshe.com/reaction/729387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Amino-4,5-difluorobenzoic acidHCID 735965—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product2-Cyclopropylamino-4,5-difluorobenzoic acidHCID 1499747394.8%

Reaction Steps

To a solution of 4,5-difluoroanthranilic acid (1.13 g, 6.53 mmol) in anhydrous methanol (40 mL) is added molecular sieves (3 Å), acetic acid (3.70 mL, 65.3 mmol) and [(1-ethoxycyclopropyl)oxy]trimethylsilane (5.25 mL, 26.11 mmol). After 30 minutes, sodium cyanoborohydride (2.08 g, 32.64 mmol) is added, and the reaction mixture is heated to reflux. After 16 hours, the reaction is cooled to room temperature, filtered, washed with methanol, and the combined filtrate concentrated under vacuum to afford a viscous oil. The resulting oil is dissolved in ethyl acetate and washed with 1.0 M hydrochloric acid, water, and brine. The organic layer is dried over MgSO4, filtered, and the filtrate is concentrated under vacuum to afford as a beige solid (1.32 g). MS CI: m/z 212 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582627B2
Source datasetuspto-grants-2009_09
ORD IDord-683fbc7e9aab429c86e45384ee7f4e3a
Source noteuspto-grants-2009_09