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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529921Generated: October 28, 2026

Triethylamine → HCID 86635088, compound

https://huagongshe.com/reaction/529921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthylamine, 2-azido-HCID 55649—
ReactantHCID 10856089HCID 10856089—
ReactantN-(2-azidoethyl)tetradecanamideHCID 57914356—
SolventDichloromethaneHCID 6344—
ProductHCID 86635088HCID 8663508855%

Reaction Steps

As in the synthesis of N-(2-azidoethyl)tetradecanamide, (E)-4-phenylbut-3-enoyl chloride (0.198 g, 1.19 mmol) was reacted with 2-azidoethanamine (0.114 g, 1.19 mmol) and triethylamine (0.239 g, 2.37 mmol) in dichloromethane (5 mL) to give (E)-N-(2-azidoethyl)-4-phenylbut-3-enamide (0.168 g, 55% yield). 1H NMR (300 MHz, CDCl3) δ 7.68 (d, J=15.6 Hz, 1H), δ 7.45 (d, J=3.3 Hz, 2H), δ 7.29 (m, 3H), δ 7.04 (t, J=4.1 Hz, 1H), δ 6.59 (d, J=15.9 Hz, 1H), δ 3.55 (q, J=6.0, 5.1 Hz, 2H), δ 3.47 (t, J=1.5 Hz, 2H) ppm; 13C NMR (75 MHz, CDCl3) δ 166.9, 141.6, 134.9, 130.1, 129.1, 128.1, 120.8, 51.1, 39.4 ppm; HRMS (ESI) calcd for C11H12N4O (M+) 216.1011. found 216.1005.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351491B2
Source datasetuspto-grants-2016_05
ORD IDord-fb5d4f19711d4f12abedd6b3c248473a
Source noteuspto-grants-2016_05