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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463841Generated: November 2, 2026

Triethylamine → HCID 53819561, compound

https://huagongshe.com/reaction/1463841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCinnamyl AlcoholHCID 5315892—
Reactant1,2,3-Benzothiadiazole-7-carbonyl chlorideHCID 18377607—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 53819561HCID 53819561—

Reaction Steps

3 g of benzo-1,2,3-thiadiazole-7-carboxylic acid chloride in 25 ml of dichloromethane are added dropwise at 15° C., with cooling and stirring, to a solution of 2.3 g of cinnamic alcohol, 3.5 g of triethylamine and a spatula tip of 4-dimethylaminopyridine in 13 ml of dichloromethane, the mixture is stirred for 16 hours at room temperature, ice-water is added, and the aqueous phase is extracted with dichloromethane. The extracts are washed with water, dried over Na2SO4 and concentrated by evaporation. The solid residue is triturated with a small amount of diethyl ether, yielding the title compound with a melting point of 70°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302607
Source datasetuspto-grants-1994_04
ORD IDord-09b71fe41a0b485f8786ab6f98454ec5
Source noteuspto-grants-1994_04