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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529929Generated: October 30, 2026

Triethylamine → HCID 57914349, compound

https://huagongshe.com/reaction/529929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthylamine, 2-azido-HCID 55649—
Reactant4-Heptylbenzoyl chlorideHCID 170864—
ReactantN-(2-azidoethyl)tetradecanamideHCID 57914356—
SolventDichloromethaneHCID 6344—
ProductHCID 57914349HCID 5791434975%

Reaction Steps

As in the synthesis of N-(2-azidoethyl)tetradecanamide, 4-heptylbenzoyl chloride (0.289 g, 1.21 mmol) was reacted with 2-azidoethanamine (0.104 g, 1.21 mmol) and triethylamine (0.245 g, 2.42 mmol) in dichloromethane (5 mL) to give N-(2-azidoethyl)-4-heptylbenzamide (0.260 g, 75% yield). 1H NMR (300 MHz, CDCl3) δ 7.73 (d, J=7.8 Hz, 2H), δ 7.19 (d, J=7.8 Hz, 3H), δ 3.57 (q, J=5.7, 5.4 Hz, 2H), δ 3.47 (t, J=5.7 Hz, 2H), δ 2.61 (t, J=7.5 Hz, 2H), δ 1.61 (m, 2H), δ 1.26 (m, 8H), δ 0.87 (t, J=6.0 Hz, 3H) ppm; 13C NMR (75 MHz, CDCl3) δ 168.3, 147.3, 131.7, 128.8, 127.4, 50.9, 39.7, 36.1, 32.0, 31.4, 29.4, 29.3, 22.9, 14.3 ppm; HRMS (ESI) calcd for C16H24N4O (M+) 288.1950. found 288.1943.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351491B2
Source datasetuspto-grants-2016_05
ORD IDord-1ab5733c6ade4b3798f8f14f3c94bfc0
Source noteuspto-grants-2016_05