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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247688Generated: October 26, 2026

Triphenylphosphine → {4-[3,3-Bis-(2-furanyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester

https://huagongshe.com/reaction/1247688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant3,3-Bis-(2-furanyl)-prop-2-en-1-olHCID 21907760—
ReactantEthyl [4-sulfanyl-2-(trifluoromethyl)phenoxy]acetateHCID 59516001—
SolventTetrahydrofuranHCID 8028—
Product{4-[3,3-Bis-(2-furanyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl esterHCID 68577859—

Reaction Steps

To a solution of 3,3-bis-(2-furanyl)-prop-2-en-1-ol (104 mg, 0.55 mmol) and triphenylphosphine (275 mg, 1.09 mmol) in THF (10 ml) was added, at room temperature and under nitrogen atmosphere, DEAD (190 mg, 1.09 mmol). The reaction mixture was stirred for 5 min after which (2-trifluoromethyl4-mercapto-phenoxy)-acetic acid ethyl ester (230 mg, 0.82 mmol) was added over 15 min. The reaction mixture was stirred at 0oC for 2 hours followed by 18 hours at room temperature and 3 hours at 50° C. The reaction mixture was evaporated and the crude residue was purified on column chromatography using ethyl acetate as eluent. The desired {4-[3,3-bis-(2-furanyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester was isolated in 11 mg yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129268B2
Source datasetuspto-grants-2006_10
ORD IDord-f424a99be8ed4ead94c7c10705857c11
Source noteuspto-grants-2006_10