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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558289Generated: October 29, 2026

Triphenylphosphine → HCID 21949861, compound

https://huagongshe.com/reaction/558289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-CyanophenolHCID 13019—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 21949766HCID 21949766—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21949861HCID 2194986149.2%

Reaction Steps

4-Hydroxy-benzonitrile (49 mg, 0.41 mmol), triphenylphosphine (106 mg, 0.41 mmol) and diethylazodicarboxylate (65 μl, 0.41 mmol) were added sequentially to a solution of the alcohol from Example 148 (74 mg, 0.27 mmol) in tetrahydrofuran (2 ml) under nitrogen at 0° C. The reaction was allowed to warm to room temperature and was stirred for 18 hours. The mixture was concentrated under reduced pressure and purified by flash chromatography on silica gel eluting with toluene:ethyl acetate (75:25, by volume) to provide the title compound (50 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063044B2
Source datasetuspto-grants-2011_11
ORD IDord-729258a4ae9d425680ecd4d942845c42
Source noteuspto-grants-2011_11