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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111671Generated: October 30, 2026

Triethylamine → 5-(tert-Butoxycarbonylaminomethyl)-3-phenylisoxazole

https://huagongshe.com/reaction/2111671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-hydroxybenzenecarboximidoyl chlorideHCID 2756315—
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
SolventTetrahydrofuranHCID 8028—
Product5-(tert-Butoxycarbonylaminomethyl)-3-phenylisoxazoleHCID 6728379254%

Reaction Steps

A solution of α-chlorobenzaldehyde oxime (Method 22; 1 g, 6.4 mmol) in THF (13 ml) was added dropwise to a solution of N-tert-butoxycarbonyl-propargylamine (0.5 g, 3.2 mmol) and triethylamine (0.9 ml, 6.4 mmol) in THF (25 ml) cooled with an ice bath. The mixture was allowed to warm to ambient temperature and stirred for 2 days. The volatiles were removed by evaporation and the residue dissolved in DCM. The solution was washed with water and brine, dried (MgSO4) and the solvent removed by evaporation. The residue was triturated with isohexane/ether (9:1) and collected by filtration to give the title compound (473 mg, 54%). NMR (CDCl3) 1.45 (s, 9H), 4.45 (d, 2H), 5.10 (bs, 1H), 6.5 (s, 1H), 7.42 (m, 3H), 7.8 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521453B2
Source datasetuspto-grants-2009_04
ORD IDord-b58b1f272343400a9b2fbe052cc1e33a
Source noteuspto-grants-2009_04