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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039489Generated: November 2, 2026

Triphenylphosphine → HCID 131728886, compound

https://huagongshe.com/reaction/1039489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantMethyl 2-(4-hydroxy-2-methylphenoxy)acetateHCID 23549552—
ReactantHCID 67145966HCID 67145966—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131728886HCID 131728886—

Reaction Conditions

Temperature0 °C

Reaction Steps

The above allyl alcohol (0.98 g, 2.60 mmol), methyl (4-hydroxy-2-methylphenoxy)acetate (0.545 g, 2.78 mmol; compound VÚFB-21004) and triphenylphosphine (0.782 g, 2.98 mmol) were dissolved in a mixture of anhydrous toluene (12 mL) and tetrahydrofuran (4 mL). The mixture was cooled to 0° C., kept under nitrogen and a degassed solution of diisopropyl azodicarboxylate (0.587 mL, 2.98 mmol) in anhydrous tetrahydrofuran (5 mL) was added dropwise. The reaction mixture was allowed to warm up to ambient temperature and then was stirred over night. The solvents were evaporated in vacuo and the residue was submitted to flash column chromatography (silica gel Fluka 60, hexanes/ethyl acetate 8:1) affording methyl (Z)-[4-[3-(4-cyclopropylphenyl)-3-(4-iodophenyl)allyloxy]-2-methylphenoxy]-acetate as solid mass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551993B2
Source datasetuspto-grants-2013_10
ORD IDord-96cdb3623b7c4c708c19a5389178147d
Source noteuspto-grants-2013_10