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HRID 520359Erstellt: 25. Oktober 2026

tert-Butylsulfinamide, (S)-(-)- → (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate

https://huagongshe.com/reaction/520359

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
EduktEthyl 4-fluoro-3,3-dimethyl-2-oxobutanoateHCID 86690078—
KatalysatorHCID 178477244HCID 178477244—
LösungsmittelSodium ChlorideHCID 5234—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoateHCID 8669007930,2%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a solution of ethyl 4-fluoro-3,3-dimethyl-2-oxobutanoate (2.3 g, 13.05 mmol) in THF (20 mL) was added (S)-2-methylpropane-2-sulfinamide (1.899 g, 15.67 mmol) and tetraethoxytitanium (5.91 mL, 26.1 mmol). The reaction mixture was heated at 65° C. for 6 h. The reaction mixture was cooled down, diluted with EtOAc and sat. NaCl (40 mL) and stirred at rt for 0.5 h. The solid was filtered and washed with water and EtOAc. The filtrate was separated and the organic layer was washed with water, sat. NaCl, dried (MgSO4) and purified by flash chromatography (EtOAc/hexane) to afford (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate (1.1 g). 1H NMR (400 MHz, CDCl3) δ ppm 4.46-4.53 (1H, m), 4.28-4.42 (3H, m), 1.59 (3H, s), 1.21-1.31 (15H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09326973B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-123710cb3b9642a2a1939182945b1418
Quellennotizuspto-grants-2016_05