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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779954Generated: November 4, 2026

Triethylamine → 3-Cyclohexyl-5-hydroxymethyl-quinoline

https://huagongshe.com/reaction/1779954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant3-Cyclohexyl-quinoline-5-carboxylic acidHCID 19048729—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-Cyclohexyl-5-hydroxymethyl-quinolineHCID 1904872681.8%

Reaction Steps

33.6 g (131.7 mmol) of the compound from Example VI are dissolved in 320 ml of dimethoxyethane and the solution is stirred with 197.6 mmol (27.6 ml) of triethylamine. After 30 minutes, 19.75 ml (197.5 mmol) of ethyl chlorocarbonate are added dropwise at 20°-30° C. The mixture is subsequently stirred for 30 minutes and the salt is filtered off with suction and washed with dimethoxyethane. The filtrate is concentrated end the residue is dissolved in a mixture of 320 ml of ethanol and 160 ml of water, and a solution of 9.25 g of sodium borohydride in 54 ml of water is added dropwise at 15°-18° C. The mixture is stirred at room temperature for 1 hour and the salt is filtered off with suction and washed with ethanol and water. The filtrate is concentrated to one third, methylene chloride and water are added and the phases are separated. The organic phase is washed 3 times with water, dried and concentrated. 26 g of a pale brown oil are obtained, which is employed without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629320
Source datasetuspto-grants-1997_05
ORD IDord-ca4926549f3a4401aa55365334230e90
Source noteuspto-grants-1997_05