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HRID 481374Erstellt: 25. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 3-(3,4-Difluorophenoxy)-5,5-dimethyl-4-(4-(methylsulfonyl)phenyl)-5H-furan-2-one

https://huagongshe.com/reaction/481374

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt2-(3,4-Difluorophenoxy)acetic acidHCID 302915—
Edukt2-Hydroxy-2-methyl-1-(4-(methylsulfonyl)phenyl)propan-1-oneHCID 15428514—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(3,4-Difluorophenoxy)-5,5-dimethyl-4-(4-(methylsulfonyl)phenyl)-5H-furan-2-oneHCID 9908624—

Reaktionsschritte

A solution of 3,4-difluorophenoxyacetic acid (0.5 1 g, 2.73 mmol), 2-hydroxy-2-methyl-1-(4-(methylsulfonyl)phenyl)propan- l-one (0.5 g, 2.1mmol, Step 3), CMC (1.13 g, 2.73mmol) and DMAP (15 mg, 0.10 mmol) in dichloromethane (12 ml) was stirred at r.t. for 18 hrs. Then, DBU (0.63 ml, 4.2 mmol) was added and the reaction mixture was refluxed for 3 h. After cooling to r.t.the mixture was extracted with ethyl acetate and washed successively with water, IN HCl and brine. The organic layer was dried over MgSO4, filtered and the solvent evaporated under vacuum. The residue was triturated in a mixture of ethyl acetate and hexane affording the title compound as a solid. M.P.: 93-95° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05789413
Quelldatensatzuspto-grants-1998_08
ORD IDord-ad470cad423f46fd8a11190d3a86e052
Quellennotizuspto-grants-1998_08