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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476770Generated: October 25, 2026

Hydrochloric Acid → 3-Chloro-2,4,5-trifluorobenzoic Acid

https://huagongshe.com/reaction/476770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant3-Amino-2,4,5-trifluorobenzoic acidHCID 2735946—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product3-Chloro-2,4,5-trifluorobenzoic AcidHCID 2734269—

Reaction Steps

A solid mixture of 0.52 g of 3-amino-2,4,5-trifluorobenzoic acid (Example 2) and 0.33 g of sodium nitrite is added in portions to a solution of 3 g of cupric chloride in 9 ml of water and 0.5 g of a 36% aqueous solution of hydrochloric acid. The resulting mixture is allowed to stir at 15°-25° C. for 1.5 hours and then additional water (25 ml) is added. Stirring is continued another hour at 25° C. and then 20 ml of diethyl ether is added. The layers are separated and the aqueous layer extracted with 20 ml of diethyl ether. The combined organic extracts are extracted with 5 ml of a 36% aqueous solution of hydrochloric acid and then concentrated on the rotary evaporator to give 0.45 g of 3-chloro-2,4,5-trifluorobenzoic acid as a tan solid; gas chromatography (GC) (98.8%); high performance liquid chromatography (HPLC) (84.8%); (a portion of the 3-chloro- 2,4,5-trifluorobenzoic acid was recrystallized from heptanes; mp 109°-111° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885386
Source datasetuspto-grants-1989_12
ORD IDord-8723184e533c4371a4518ae1b250751d
Source noteuspto-grants-1989_12