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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023845Generated: November 1, 2026

2-Iodophenol → HCID 67206796, compound

https://huagongshe.com/reaction/1023845

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodophenolHCID 10784—
ReactantTriphenylphosphineHCID 11776—
Reactanto-(Trifluoromethyl)phenethyl alcoholHCID 587845—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67206796HCID 6720679656%

Reaction Steps

To a stirred solution of the 2-iodophenol (220.0 mg, 1.0 mmol), the 2-(2-(trifluoromethyl)phenyl)ethanol (228.0 mg, 1.2 mmol), and triphenyl phosphine (314.0 mg, 1.2 mmol) in anhydrous THF (5 mL) at 0° C. was added DEAD (40% in toluene, 1.20 mmol, 0.35 mL) dropwise. The yellow solution was allowed to warm to room temperature and stirring was continued overnite. After evaporating the solvent under reduced pressure the crude residue was dissolved in DCM (15 mL). The organic layer was washed with 10% NaOH (2×10 mL), water and brine. The organic phase was dried (Na2SO4), filtered and evaporated under reduced pressure. The crude residue was purified by column chromatography on silica gel using hexanes/EtOAc as the eluent. The compound was isolated in 56% yield as a white solid. 1H NMR: 3.17 (t, 2H, J=6.8 Hz), 4.22 (t, 2H, J=6.8 Hz), 6.90-7.10 (m, 4H), 7.15-7.23 (m 1H), 7.30-7.45 (m, 2H), 7.74 (dd, 1H, J=7.6, 1.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722720B2
Source datasetuspto-grants-2014_05
ORD IDord-877d5f5a1a9a468c93bfb2ec00ff8b39
Source noteuspto-grants-2014_05