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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437598Generated: November 1, 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/1437598

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 h. 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 MHz): 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, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622502B2
Source datasetuspto-grants-2009_11
ORD IDord-7e0be04b47bb47d98519ae00bba8f224
Source noteuspto-grants-2009_11