Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111674Generated: October 31, 2026

Triethylamine → Ethyl 5-(N-Boc)aminomethylisoxazole-3-carboxylate

https://huagongshe.com/reaction/2111674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-chloro-2-(hydroxyimino)acetateHCID 6399471—
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-(N-Boc)aminomethylisoxazole-3-carboxylateHCID 1058809660%

Reaction Steps

A solution of ethyl chlorooximidoacetate (10 g, 66 mmol) in THF (200 ml) was added dropwise over 3 hours to a mixture of N-(tert-butyloxycarbonyl)propargylamine (20.5 g, 131 mmol) and triethylamine (11.2 ml, 80 mmol) in tetrahyrofuran (100 ml). The mixture was stirred at ambient temperature for 18 hours and then the volatiles were removed by evaporation. The residue was dissolved in DCM and washed with water followed by brine. The organics were separated, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography on silica gel eluting with isohexane/diethyl ether (80:20 then 50:50) to give the title compound (10.6 g, 60%). NMR (DMSO): 1.3 (t, 3H), 1.38 (s, 9H), 4.35 (m, 2H), 6.62 (s, 1H), 7.55 (s, 1H); m/z 269 (M−H)—.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521453B2
Source datasetuspto-grants-2009_04
ORD IDord-7f84297867654b40b98f3ebe1f43cae8
Source noteuspto-grants-2009_04