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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549873Generated: October 30, 2026

Triphenylphosphine → HCID 131728886, compound

https://huagongshe.com/reaction/549873

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 numberUS07943613B2
Source datasetuspto-grants-2011_05
ORD IDord-2844486d2b0a4034ad4fe00336af0379
Source noteuspto-grants-2011_05