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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247518Generated: October 26, 2026

Hydrochloric Acid → 4'-Hexyl-4-biphenylcarboxylic acid 3-chloro-4-[(3-chloro-4-cyanophenoxy)carbonyl]phenyl ester

https://huagongshe.com/reaction/247518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-4-hydroxybenzonitrileHCID 592797—
Reactant2-Chloro-4-[[p-(p-hexylphenyl)benzoyl]oxy]benzoyl chlorideHCID 20159497—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
Product4'-Hexyl-4-biphenylcarboxylic acid 3-chloro-4-[(3-chloro-4-cyanophenoxy)carbonyl]phenyl esterHCID 53821925—

Reaction Conditions

Temperature65 °C

Reaction Steps

The crude 2-chloro-4-{[p-(p-hexylphenyl)benzoyl]oxy}benzoyl chloride obtained was dissolved in 125 ml of benzene and then added dropwise to a solution of 4.0 g of 3-chloro-4-cyanophenol in 100 ml of pyridine. The mixture was stirred at a bath temperature of 65° C. overnight, then poured into ice-cold, dilute hydrochloric acid and extracted with diethyl ether. The extract was washed several times with 3N hydrochloric acid, then washed neutral with water, dried and evaporated. The crude 4'-hexyl-4-biphenylcarboxylic acid 3-chloro-4-[(3-chloro-4-cyanophenoxy)carbonyl]phenyl ester obtained was chromatographed on silica gel with toluene/dichloromethane (1:1). The fractions (8.2 g) which were practically pure according to thin-layer chromatography were recrystallized once from ethyl acetate and once from ethyl acetate and a small amount of hexane; m.p. (C-N) 95° C., cl.p. (N-I) 235° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04708441
Source datasetuspto-grants-1987_11
ORD IDord-25bfb25d4d0c46e59a7483fae39bf83b
Source noteuspto-grants-1987_11