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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810665Generated: November 3, 2026

Triphenylphosphine → HCID 131728886, compound

https://huagongshe.com/reaction/1810665

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 numberUS08362016B2
Source datasetuspto-grants-2013_01
ORD IDord-9ac9d4406168445b9fc7a4717fc91a40
Source noteuspto-grants-2013_01