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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919770Generated: October 26, 2026

Triphenylphosphine → 5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pent-2-yl acetate

https://huagongshe.com/reaction/1919770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant5-Hydroxypent-2-yl acetateHCID 15128952—
Reactant4-(1,1,1,3,3,3-Hexafluoro-2-(methoxymethoxy)propan-2-yl)-2-propylphenolHCID 59201037—
ReactantN-ethoxycarbonyliminocarbamateHCID 86599450—
SolventTetrahydrofuranHCID 8028—
Product5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pent-2-yl acetateHCID 5923513385%

Reaction Steps

5-Hydroxypent-2-yl acetate (58.5 mg), triphenylphosphine (131 mg) and ethyl azodicarboxylate (2.2 mol/L, 200 μL) were added to a mixed solution of 4-[1,1,1,3,3,3-hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenol (69.3 mg, 200 μmol) in tetrahydrofuran (2 mL) at room temperature. After completion of the reaction, the solvent was evaporated, and the residue was purified by silica gel preparative thin-layer chromatography (hexane:ethyl acetate=5:1) to obtain 80.4 mg of the title compound (yield: 85%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168666B2
Source datasetuspto-grants-2012_05
ORD IDord-1c70ace4880e4db0b928ab9eb0ef2bac
Source noteuspto-grants-2012_05