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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762022Generated: October 30, 2026

HCID 13463460, compound → HCID 178444426, compound

https://huagongshe.com/reaction/1762022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13463460HCID 13463460—
ReactantHCID 178444415HCID 178444415—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
ProductHCID 178444426HCID 178444426—

Reaction Steps

The crude (S)-4-(6-methyloctyloxy)benzoyl chloride obtained was dissolved in 20 ml of toluene and then added dropwise to a solution of 0.26 g of 4-[2-(trans-4-pentylcyclohexyl)ethyl]phenol in 2 ml of pyridine. The reaction mixture was stirred at room temperature overnight, then poured into ice-water and extracted with diethyl ether. The extract was washed four times with 25 ml of 1N hydrochloric acid each time, then washed with 25 ml of 2N sodium carbonate solution and several times with water, dried over magnesium sulphate and concentrated. Chromatography of the residual oil on silica gel with toluene gave 0.2 g of (S)-4-(6-methyloctyloxy)benzoic acid 4-[2-(trans-4-pentylcyclohexyl)ethyl]phenyl ester. The product was recrystallized several times from ethanol until the phase transition temperatures were constant. M.p. (C-S) 58°, transition S-S*C 58.5° C., transition S*C -Ch 93° C., cl.p. (CH-I) 140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04830470
Source datasetuspto-grants-1989_05
ORD IDord-17dcfdb9a7a7420198e6915af56c14fe
Source noteuspto-grants-1989_05