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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733404Generated: October 30, 2026

2,5-Dichlorobenzoic acid → HCID 20298962, compound

https://huagongshe.com/reaction/1733404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichlorobenzoic acidHCID 5784—
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantSodium hydrideHCID 24758—
SolventO-XyleneHCID 7237—
ProductHCID 20298962HCID 2029896232.6%

Reaction Steps

2,5-Dichlorobenzoic acid (5 g) and 3-trifluoromethylphenol (4.24 g) were dissolved in xylene and the solution placed under dry oxygen-free nitrogen. Sodium hydride (1.25 g) was slowly added and when effervescence had ceased, cuprous bromide was added and the solution or suspension refluxed for 6 hours. The xylene was removed by low pressure distillation. The solid residue was treated with water and acidified with dilute hydrochloric acid. The resulting oil was extracted into diethyl ether and the ether removed by low pressure distillation to give a light yellow solid which was recrystallised from diethyl ether/petroleum ether to give the title compound (2.7 g), mp, 124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242121
Source datasetuspto-grants-1980_12
ORD IDord-01cf0b4a2867480f905e3a18fe4c50c4
Source noteuspto-grants-1980_12