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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258135Generated: November 2, 2026

Triethylamine → HCID 73234970, compound

https://huagongshe.com/reaction/1258135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAziridine, 2-(1,3-benzodioxol-5-yl)-HCID 12316717—
ReactantHCID 67043436HCID 67043436—
SolventTetrahydrofuranHCID 8028—
ProductHCID 73234970HCID 7323497085%

Reaction Conditions

Temperature25 °C

Reaction Steps

Triethylamine (0.4 mL, 3.0 mmol, 2.0 equiv) and β-chloroenone 53 (280 mg, 1.5 mmol, 1.0 equiv) were sequentially added to a stirred solution of aziridine 15 (360 mg, 2.2 mmol, 1.5 equiv) in tetrahydrofuran (10 mL) at 25° C. The resulting white mixture was stirred at 25° C. for 3 h. The crude reaction mixture was loaded directly onto a column and purified by silica gel column chromatography (1% triethylamine and 49% benzene in ethyl acetate) to afford 54 (400 mg, 85% yield) as a yellow foam. Rf=0.68 (1% triethylamine and 49% benzene in ethyl acetate); 1H NMR (500 MHz, C6D6) δ 6.55-6.70 (m, 3H, ArH), 5.24-5.28 (m, 2H, OCH2O), 5.14-5.18 (m, 1H, NCCH), 4.50-4.56 (m, 1H, CH(OR)), 4.19-4.27 (m, 1H, CH(OR)), 2.46-3.18 (m, 1H, ArCHN), 1.84-2.17 (m, 1H, CH2N), 1.63-1.78 (m, 1H, CH2N), 1.28-1.32 (m, 3H, CH3), 1.10-1.12 (m, 3H, CH3); IR (neat film) 2989 (w), 1703 (m), 1586 (s) cm−1; HRMS (ESI) m/z: Calcd for C17H18NO5 (MO 316.1185; observed 316.1186.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466142B2
Source datasetuspto-grants-2013_06
ORD IDord-e1d130addbca4ee2a41aa1ef437cf719
Source noteuspto-grants-2013_06