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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715680Generated: October 30, 2026

Triphenylphosphine → HCID 58072009, compound

https://huagongshe.com/reaction/715680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTetrahydro-4H-pyran-4-olHCID 74956—
Reactant4-hydroxy-3-(trifluoromethyl)benzonitrileHCID 2783159—
ReactantDi-tert-butyl diazene-1,2-dicarboxylateHCID 6034084—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58072009HCID 58072009—

Reaction Steps

2 g 4-Hydroxy-3-trifluoromethyl-benzonitrile, 5.6 g triphenylphosphine and 1.2 g tetrahydro-4H-pyran-4-ol was suspended in 15 mL tetrahydrofuran at 0° C. before 4.92 g di-tert-butylazodicarboxylate (DBAD) as a solution in 5 mL tetrahydrofuran was added over 15 min. The reaction was warmed to ambient temperature. Additional 2.8 g triphenylphosphine, 0.55 g (5.3 mmol) tetrahydro-4H-pyran-4-ol and 2.46 g di-tert-butylazodicarboxylate (DBAD) in tetrahydrofuran were added and the reaction was stirred overnight. After this time, the reaction was diluted with water and extracted with ethyl acetate (×2). The organic phase was separated and then it was washed with 2N sodium hydroxide, water and saturated sodium chloride, dried over sodium sulfate, filtered and the filtrate was concentrated under reduced pressure. The residue was purified with silica gel chromatography (SiO2: heptane/ethyl acetate) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187478B2
Source datasetuspto-grants-2015_11
ORD IDord-59d82300d8bb4e21a896daf231d8eb69
Source noteuspto-grants-2015_11