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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816728Generated: November 2, 2026

Triphenylphosphine → HCID 54308849, compound

https://huagongshe.com/reaction/1816728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantMethyl 4'-hydroxy(1,1'-biphenyl)-4-carboxylateHCID 1490289—
Reactant(S)-(-)-2-(tert-Butoxycarbonylamino)-3-cyclohexyl-1-propanolHCID 11043405—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 54308849HCID 5430884916%

Reaction Steps

To a solution of methyl 4-(4-hydroxyphenyl)benzoate (0.94 g), (S)-(−)-2-(tert-butoxycarbonylamino)-3-cyclohexyl-1-propanol (1.00 g) and triphenylphosphine (1.62 g) in N,N-dimethylformamide (20 ml) was added dropwise diisopropyl azodicarboxylate (1.21 ml) for 10 minutes under ice-cooling in a stream of nitrogen. The solution was stirred for 16 hours at ambient temperature, and then water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a mixed solvent of n-hexane-ethyl acetate (from 0% to 20% gradient elution) to give methyl (S)-4-[4-[2-(tert-butoxycarbonylamino)-3-cyclohexylpropyloxy]phenyl]benzoate (290 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884868B1
Source datasetuspto-grants-2005_04
ORD IDord-8ed2af07509c4c04af7761ae96105be3
Source noteuspto-grants-2005_04