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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870272Generated: November 1, 2026

Triphenylphosphine → 3-(2-(N-t-Butoxycarbonylamino)ethoxy)-5-chloro-1,2-benzisoxazole

https://huagongshe.com/reaction/1870272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
ReactantHCID 178518984HCID 178518984—
SolventTetrahydrofuranHCID 8028—
Product3-(2-(N-t-Butoxycarbonylamino)ethoxy)-5-chloro-1,2-benzisoxazoleHCID 1545393675.2%

Reaction Steps

To a solution of triphenylphosphine (0.87 g) in tetrahydrofuran (10 ml), was added diethyl azodicarboxylate (0.57 g) dropwise with stirring under ice cooling. The reaction mixture was stirred at the same temperature for 10 minutes. Then, 2-(N-t-butoxycarbonylamino)ethanol (0.48 g) and 5-chloro-3-hydroxy-1,2-benzisoxazole (0.51 g) were added to the reaction mixture successively and stirred under ice cooling for 10 minutes and at room temperature for 24 hours. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography with cyclohexane/ethyl acetate (4/1) as an eluent. The title compound (0.70 g) was obtained as colorless crystals by crystallization from isopropylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096771
Source datasetuspto-grants-2000_08
ORD IDord-feb141ee5c10430b9e0c2c61800d8af4
Source noteuspto-grants-2000_08