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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337255Generated: October 28, 2026

Triphenylphosphine → 3-(3-(2,6-Dimethylbenzyloxy)phenyl)propanenitrile

https://huagongshe.com/reaction/337255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(2,6-Dimethylphenyl)methanolHCID 186748—
Reactant3-(3-Hydroxyphenyl)propanenitrileHCID 1712312—
SolventTetrahydrofuranHCID 8028—
Product3-(3-(2,6-Dimethylbenzyloxy)phenyl)propanenitrileHCID 66959389—

Reaction Steps

A solution of 3-(3-hydroxyphenyl)propanenitrile (Step B, 1.25 g, 8.5 mmol) and diisopropyl azodicarboxylate (DIAD, 1.87 g, 9.26 mmol) in dry THF (10 ml) was added drop wise to a solution of 2,6-Dimethylbenzyl alcohol (1.27 g, 9.3 mmol) and triphenylphosphine (TPP, 2.43 g, 9.26 mmol) in dry THF (30 ml) at 0° C. under argon. The reaction mixture was warmed to room temperature for 4 hours or until all the starting material is consumed, diluted with ether and washed with water (2×). The organic layer was dried over Na2SO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (hex: ethyl acetate 2:1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889724B2
Source datasetuspto-grants-2014_11
ORD IDord-56fc9acd305a4bdb9d2318da9900a240
Source noteuspto-grants-2014_11