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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198830Generated: November 2, 2026

Triethylamine → HCID 54190974, compound

https://huagongshe.com/reaction/1198830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium AzideHCID 33557—
Reactant4-(5-pentylpyridin-2-yl)benzoic acidHCID 2053671—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 54190974HCID 5419097493.7%

Reaction Steps

A solution of 2.1 g of p-(5-pentyl-2-pyridyl)benzoic acid in 80 ml of acetone was cooled to 2° C. while stirring and gassing with nitrogen and treated dropwise within 10 minutes with a solution of 2.16 ml of triethylamine in 15 ml of acetone. The reaction mixture was then treated dropwise at 1°-2° C. within 10 minutes with a solution of 1.86 ml of ethyl chloroformate in 8 ml of acetone and stirred at this temperature for a further 30 minutes. Subsequently, a solution of 1.38 g of sodium azide in 8 ml of water was added dropwise to the reaction mixture at 1°-2° C. within 10 minutes and the resulting mixture was stirred for a further 1 hour in an ice-bath. Thereafter, the reaction mixture was poured into 200 ml of water and extracted with diethyl ether. The organic phase was washed with water, dried over sodium sulphate, filtered and freed from solvent. Purification of the resulting light yellowish crystals (2.1 g) by chromatography on 120 g of silica gel with 1 l of methylene chloride gave 2.15 g of p-(5-pentyl-2-pyridyl)benzoic acid azide as a light yellowish paste.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898455
Source datasetuspto-grants-1990_02
ORD IDord-dc94d4aab95a4184a927b8873dfc678d
Source noteuspto-grants-1990_02