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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865805Generated: November 1, 2026

Triethylamine → HCID 86048447, compound

https://huagongshe.com/reaction/1865805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAziridineHCID 9033—
ReactantHCID 86048448HCID 86048448—
SolventEthyl AcetateHCID 8857—
ProductHCID 86048447HCID 8604844784.3%

Reaction Steps

A solution of 2-chloro-N-(6-hydroxyhexyl)-3,5-dinitrobenzamide (16) [for preparation see Example 14 below] (118 mg, 0.34 mmol) and Et3N (200 mg) in EtOAc (200 mL) was treated with aziridine (100 mg) at room temperature for 3 h. The mixture was diluted with EtOAc and washed three times with water, after dry, concentrated under reduced pressure until about 20 mL, the yellow solid was collected and gave 101 mg product (84%); 1H NMR [(CD3)2SO] δ 8.74 (d, J=2.8 Hz, 1 H), 8.63 (m, 1 H), 8.29 (d, J=2.8 Hz, 1 H), 4.31 (m, 1 H), 3.39 (m, 2 H), 3.25 (m, 2 H), 2.37 (s, 4 H), 1.56 (m, 2 H), 1.43 (m, 2 H), 1.33 (m, 4 H). Anal. (C15H20N4O6) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629332B2
Source datasetuspto-grants-2009_12
ORD IDord-79ff7128d62847659b01a55b63d70328
Source noteuspto-grants-2009_12