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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039533Generated: November 1, 2026

Triphenylphosphine → methyl (E)-[4-[3-(4-bromophenyl)-3-[4-trifluoromethylphenyl]allyloxy]-2-methylphenoxy]acetate

https://huagongshe.com/reaction/1039533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(E)-3-(4-bromophenyl)-3-(4-trifluoromethylphenyl)-prop-2-en-1-olHCID 19261649—
ReactantMethyl 2-(4-hydroxy-2-methylphenoxy)acetateHCID 23549552—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Productmethyl (E)-[4-[3-(4-bromophenyl)-3-[4-trifluoromethylphenyl]allyloxy]-2-methylphenoxy]acetateHCID 131728891—

Reaction Conditions

Temperature0 °C

Reaction Steps

The above allyl alcohol (0.77 g, 2.16 mmol), methyl (4-hydroxy-2-methylphenoxy)acetate (0.47 g, 2.37 mmol) and triphenylphosphine (0.68 g, 2.59 mmol) were dissolved in a mixture of anhydrous toluene (10 mL) and tetrahydrofuran (3 mL). The mixture was degassed, cooled to 0° C. and a degassed solution of diisopropyl azodicarboxylate (0.525 g, 2.60 mmol) in anhydrous tetrahydrofuran (3 mL) was added dropwise under nitrogen. The reaction mixture was stirred at ambient temperature over night. The solvents were evaporated in vacuo and the residue was submitted to column chromatography (silica gel Fluka 60, hexanes/ethyl acetate 95: 5-90:10) affording methyl (E)-[4-[3-(4-bromophenyl)-3-[4-trifluoromethylphenyl]allyloxy]-2-methylphenoxy]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551993B2
Source datasetuspto-grants-2013_10
ORD IDord-9f3f9ebea3c44310a980efdf0a105114
Source noteuspto-grants-2013_10