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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922282Generated: October 31, 2026

Triphenylphosphine → HCID 87106278, compound

https://huagongshe.com/reaction/922282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 66685333HCID 66685333—
Reactant(4-{[(2E)-2-(methoxyimino)-2-phenylethyl]oxy}phenyl)methanolHCID 86695770—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87106278HCID 8710627821.74%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 50 mL RB flask fitted with magnetic stirrer was charged dry THF (5.0 mL) and (4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}phenyl)methanol (0.134 g, 0.5 mmol). To the above mixture methyl 3-(4-hydroxyphenyl)hexanoate (0.11 g, 0.5 mmol) was added and the resulting mixture stirred at 0° C. for 5 min. Triphenyl phosphine (0.17 g, 0.65 mmol) was added to the mixture and stirred at 0° C. for 15 min followed by the addition of diethylazadicarboxylate (0.13 g, 0.65 mmol). After stirring the resulting mixture at RT for 16 h, the RM was evaporated to remove the THF. The residue was diluted with water (15 mL) and extracted with ethyl acetate (15 mL×2). The organic layer was washed with saturated brine solution (15 mL) and dried over anhydrous Na2SO4. Concentration of the solvent and purification of the resulting residue by column chromatography on silica gel (100/200 mesh), using petroleum ether and ethyl acetate as eluent, gave the product (0.05 g, yield: 21.74%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278915B2
Source datasetuspto-grants-2016_03
ORD IDord-3adcb36ed53a404fa956e2527a522925
Source noteuspto-grants-2016_03