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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348380Generated: October 30, 2026

3-(4-Benzyloxy-phenyl)-2-(2-methoxy-phenoxy)-2-methyl-3-(2,2,2-trifluoro-acetoxy)-propionic acid ethyl ester → 3-(4-Hydroxyphenyl)-2-(2-methoxy-phenoxy)-2-methyl-propionic acid ethyl ester

https://huagongshe.com/reaction/348380

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Benzyloxy-phenyl)-2-(2-methoxy-phenoxy)-2-methyl-3-(2,2,2-trifluoro-acetoxy)-propionic acid ethyl esterHCID 69354241—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product3-(4-Hydroxyphenyl)-2-(2-methoxy-phenoxy)-2-methyl-propionic acid ethyl esterHCID 5880182425%

Reaction Steps

3-(4-Benzyloxy-phenyl)-2-(2-methoxy-phenoxy)-2-methyl-3-(2,2,2-trifluoro-acetoxy)-propionic acid ethyl ester was dissolved in ethyl acetate (350 mL), treated with 5% palladium on carbon (8.77 g), and stirred under an atmosphere of hydrogen for 48 h. The suspension was filtered through celite and concentrated in vacuo. The residue was purified by flash column chromatography (25% ethyl acetate in hexanes) to provide the title compound as a light yellow oil (1.73 g, 25%). 1H NMR (400 MHz, CDCl3): δ 7.12 (d, 2H, J=6.65 Hz), 6.98–6.93 (m, 5H), 4.24–4.15 (m, 2H), 3.75 (s, 3H), 3.23 (d; 1H, J=13.69 Hz), 3.13 (d, 1H, J=13.69 Hz), 1.30 (s, 3H), 1.22 (t, 3H, J=7.43 Hz). MS [EI+] 331 (M+H)+, [EI−] 329 (M−H)+. Rf=0.14 in 25% ethyl acetate in hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176224B2
Source datasetuspto-grants-2007_02
ORD IDord-0b29e708cd644dbda4e3ba0946de5de0
Source noteuspto-grants-2007_02