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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710202Generated: November 1, 2026

Triethylamine → HCID 178443718, compound

https://huagongshe.com/reaction/1710202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 135734288HCID 135734288—
ReactantHCID 178447990HCID 178447990—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 178443718HCID 178443718—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-(4-n-Octyloxyphenyl)-5-(4-hydroxyphenyl)-1,3,4-thiadiazole (0.1 mole, 3.82 g) is suspended in 50 mL of absolute toluene and, after addition of 10 mL triethylamine and 100 mg 4-dimethylaminopyridine, treated with stirring with 0.011 moles (2.38 g) 3-(trans-4-n-propylcyclohexyl)-propionyl chloride. The mixture is stirred for 12 hours at room temperature and for 2 hours at 80° C. After being allowed to cool to room temperature, the reaction solution is diluted with 100 mL ether and washed once with 100 mL water, once with 100 mL 5% sodium bicarbonate solution and once again with 100 mL water. After drying over Na2SO4, the solvent is distilled off in a rotary evaporator. The residue is recrystallized from ethanol and methanol until the transition temperature is constant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952699
Source datasetuspto-grants-1990_08
ORD IDord-57dd87cae94443629ad5544619a1a656
Source noteuspto-grants-1990_08