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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375705Generated: October 30, 2026

(2Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl acetate → (2Z)-4-hydroxy-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl acetate

https://huagongshe.com/reaction/1375705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl acetateHCID 58787781—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
Product(2Z)-4-hydroxy-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl acetateHCID 5878778999.9%

Reaction Steps

To a solution of 50.5 g of (2Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl acetate in 125 mL of MeCN, 10 mL of PyHF was added and the resulted mixture was stirred at rt for 1.5 hr. The reaction mixture was diluted with 600 mL of toluene and then loaded on silica gel column and eluted with EtOAc. The solvent was evaporated to afford 38.3 g of the titled compound. 1H NMR (acetone-d6, 500 M Hz): δ 7.68 (d, 2H), 7.32 (d, 2H), 7.15–7.00 (m, 5H), 5.20 (s, 2H), 4.62 (d, 2H), 4.09 (t, 1H, OH), 3.02 (s, 3H), 1.92 (s, 3 H),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169809B2
Source datasetuspto-grants-2007_01
ORD IDord-af05a29582e3402987d67f32642aaed4
Source noteuspto-grants-2007_01