Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183858Generated: November 4, 2026

Triphenylphosphine → HCID 69743753, compound

https://huagongshe.com/reaction/2183858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-Chloro-2-hydroxybenzonitrileHCID 3442789—
ReactantHCID 54753949HCID 54753949—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69743753HCID 69743753148.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

The product of step (b) (3.25 g, 13.9 mmol), 4-chloro-2-hydroxybenzonitrile (2.14 g, 13.9 mmol) and triphenylphosphine (4.38 g, 16.7 mmol) were dissolved in anhydrous tetrahydrofuran (80 ml) and the solution cooled to 0° C. Diethyl azodicarboxylate (2.91 g, 16.7 mmol) was added dropwise and the solution allowed to warm to room temperature, then stirred for 2 days. The solvent was removed in vacuo and the residue chromatographed on flash silica, eluting with hexane:ethyl acetate (3:1), to afford the title compound as a white solid (3.562 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900243B2
Source datasetuspto-grants-2005_05
ORD IDord-74d785a9db304a8a84684f86bf9ee236
Source noteuspto-grants-2005_05