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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106579Generated: October 30, 2026

Acetone → 5,5-Dimethyl-3-(3-fluorophenyl)-2-hydroxy-4-(4-methylsulfonylphenyl)-2,5-dihydrofuran

https://huagongshe.com/reaction/1106579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantPotassium sodium tartarateHCID 9855836—
Reactant5,5-dimethyl-3-(3-fluorophenyl)-4-(4-methylsulfonyl)phenyl-2(5H)-furanoneHCID 9906892—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5,5-Dimethyl-3-(3-fluorophenyl)-2-hydroxy-4-(4-methylsulfonylphenyl)-2,5-dihydrofuranHCID 9863787—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a -50° C. solution of 5,5-dimethyl-3-(3-fluorophenyl)-4-(4-(methylsulfonyl)phenyl)-2-(5H)-furanone (30 g, 83.3 mmol) in 500 mL of THF was added dropwise a solution of DIBAL (90 mL, 1.5 M in toluene) over a period of 15 min. The reaction mixture was allowed to warm to -10° C. over a period of 1 h, then treated with 20 mL of acetone, followed by 50 mL of methanol. The reaction mixture was then warmed to -20° C. and treated with aqueous potassium sodium tartrate (20%, 400 mL). After stirring at r.t. for 1 h, the product was extracted with 500 mL of 2:1 EtOAc/hexane, dried over Na2SO4, filtered and concentrated. The crude product was swished with 2:1 hexane/EtOAc to give 24 g of purified title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057319
Source datasetuspto-grants-2000_05
ORD IDord-bb807d0981cc425e904bc278f53c57a5
Source noteuspto-grants-2000_05