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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294317Generated: October 31, 2026

Triphenylphosphine → HCID 68884003, compound

https://huagongshe.com/reaction/1294317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl (2-hydroxyphenyl)acetateHCID 89719—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 68885917HCID 68885917—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 68884003HCID 6888400366%

Reaction Steps

To a mixture of [4-[(E)-2-(5-methyl-2-phenyl-4-oxazolyl)ethenyl]phenyl]methanol (0.50 g), methyl 2-(2-hydroxyphenyl)acetate (0.27 g), triphenylphosphine (0.63 g) and tetrahydrofuran (30 mL) was dropwise added a solution (40%, 1.04 g) of diethyl azodicarboxylate in toluene at room temperature, and the mixture was stirred for 15 hrs. To the reaction mixture was added ethyl acetate, the mixture was washed successively with water, a 2N aqueous sodium hydroxide solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give methyl 2-[2-[4-[(E)-2-(5-methyl-2-phenyl-4-oxazolyl)ethenyl]benzyloxy]phenyl]acetate as a pale-yellow oil (0.4-6 g, 66%) from a fraction eluted with ethyl acetate-hexane (1:6, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-d28bdf0b28b84690ae4d8d97e81c6ccc
Source noteuspto-grants-2007_07