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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375702Generated: October 26, 2026

Rofecoxib → (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol

https://huagongshe.com/reaction/1375702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRofecoxibHCID 5090—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium HydroxideHCID 14798—
SolventDichloromethaneHCID 6344—
Product(2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diolHCID 5743477398.7%

Reaction Steps

To a solution of 110 g of 4-(4-methanesulfonyl-phenyl)-3-phenyl-5H-furan-2-one in 1.5 L of dichloromethane stirred at −78° C., 150 mL of DIBAL was added dropwise. The resulting mixture was warmed to room temperature and stirred overnight. The reaction mixture was then cooled to −78° C., and 1.2 L of 1 M aqueous NaOH was added dropwise. After the addition, the resulting mixture was warmed to room temperature and the organic phase was separated. The aqueous phase was extracted with dichloromethane. The organic phases were combined and dried over Na2SO4. 110 g of the titled compound was obtained after evaporation. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2H), 7.36 (d, 2H), 7.16–7.05 (m, 5H), 4.66 (d, 2H), 4.63 (d, 2H), 4.19 (t, 1H, OH), 4.17 (t, 1 H. OH), 3.04 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169809B2
Source datasetuspto-grants-2007_01
ORD IDord-5edd1a315fdf4ebbb46c36c2676df4c7
Source noteuspto-grants-2007_01