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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956897Generated: November 1, 2026

Triphenylphosphine → HCID 73194738, compound

https://huagongshe.com/reaction/1956897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dioneHCID 2818126—
ReactantHCID 54134047HCID 54134047—
SolventTetrahydrofuranHCID 8028—
ProductHCID 73194738HCID 7319473840.3%

Reaction Steps

A solution of 450 mg of diethyl azodicarboxylate in 4 ml of tetrahydrofuran was added dropwise at room temperature to a solution of 383 mg of 2-(benzylideneaminooxy)ethanol (prepared as described in Preparation 1), 1.00 g of 5-(4-hydroxybenzyl)-3-tritylthiazolidine-2,4-dione and 629 mg of triphenylphosphine in 10 ml of tetrahydrofuran, and the resulting mixture was stirred at room temperature for 16 hours. At the end of this time, the reaction product was purified by column chromatography through silica gel, using a 3:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.53 g of the title compound as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780490
Source datasetuspto-grants-1998_07
ORD IDord-75026e21238e4f8f9cbba35c5cf396ef
Source noteuspto-grants-1998_07