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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392908Generated: October 29, 2026

Triphenylphosphine → HCID 11961748, compound

https://huagongshe.com/reaction/392908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 22661867HCID 22661867—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11961748HCID 1196174869%

Reaction Steps

Triphenylphosphine (1.64 g, 6.24 mmol) was added to a solution of 2-benzyloxy-5-cyano-benzylazide (1.1 g, 4.16 mmol) in anhydrous THF (10 mL) at 0° C. After 1 hour, ammonium hydroxide (0.5 mL) was added and the mixture was warmed to room temperature and stirred overnight. The mixture was concentrated and the residue purified by flash chromatography (3% methanol/dichloromethane) to afford 677 mg (69%) of the title compound as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.6-7.3 (m, 7H); 6.95 (d, 1H, J=9.1 Hz); 5.18 (s, 2H); 3.9 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803457B1
Source datasetuspto-grants-2004_10
ORD IDord-27140a9d3977445ca265dd4987084230
Source noteuspto-grants-2004_10