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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187947Generated: October 31, 2026

Triphenylphosphine → benzyl (3R)-3-t-butoxycarbonylamino-4-(5-cyano-2-benzyloxyphenoxy)butanoate

https://huagongshe.com/reaction/2187947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantBoc-D-aspartinol 4-Benzyl EsterHCID 11045079—
Reactant4-(Benzyloxy)-3-hydroxybenzonitrileHCID 15453451—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Productbenzyl (3R)-3-t-butoxycarbonylamino-4-(5-cyano-2-benzyloxyphenoxy)butanoateHCID 86584114—

Reaction Steps

4.8 g (15.5 mmol) of benzyl (3R)-3-t-butoxycarbonylamino-4-hydroxybutanoate was dissolved in 100 ml of tetrahydrofuran. 2.9 g (12.9 mmol) of 4-benzyloxy-3-hydroxybenzonitrile, 4.1 g (15.5 mmol) of triphenylphosphine and 6.7 g (15.5 mmol) of diethyl azodicarboxylate were added to the obtained solution under cooling with ice, and they were stirred at room temperature overnight. After the treatment with ethyl acetate as the extraction solvent in an ordinary manner, the obtained crude product was purified by the silica gel column chromatography to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410538B2
Source datasetuspto-grants-2002_06
ORD IDord-0247d63942df4e5b9572de63d156732f
Source noteuspto-grants-2002_06