Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216581Generated: October 30, 2026

Hydrochloric Acid → 4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid

https://huagongshe.com/reaction/216581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Chloro-2,4-difluoro-5-nitrobenzoic acidHCID 15549918—
SolventWaterHCID 962—
Product4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acidHCID 2111418285.8%

Reaction Steps

Ammonium hydroxide solution (6.88 g, −30% in water, 58.9 mmol) is added to a solution of 3-chloro-2,4-difluoro-5-nitro-benzoic acid 2a (3.5 g, 14.7 mmol) in water (16 mL) at 0° C. with stirring. Upon completion of the ammonium hydroxide addition the reaction mixture is warmed to room temperature. After 5 hours the reaction mixture is cooled to 0° C. and concentrated HCl is carefully added until the pH of the reaction mixture is near zero. The solid is collected by filtration and washed with water and diethyl ether. The solids are transferred to a round bottom flask as a solution in MeOH and EtOAc and concentrated under reduced pressure to give 2.96 g of a yellow solid. The filtrate is partitioned between diethyl ether and water and the organic layer is washed with brine. The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure to give 0.65 g of product. Recovered a total of 3.61 g (104%) of pure desired product that is carried forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193230B2
Source datasetuspto-grants-2012_06
ORD IDord-4ec2d07d46af4355981092608d4708d1
Source noteuspto-grants-2012_06