HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 520359Erstellt: 25. Oktober 2026
tert-Butylsulfinamide, (S)-(-)- → (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate
https://huagongshe.com/reaction/520359
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Edukt | Ethyl 4-fluoro-3,3-dimethyl-2-oxobutanoate | HCID 86690078 | — |
| Katalysator | HCID 178477244 | HCID 178477244 | — |
| Lösungsmittel | Sodium Chloride | HCID 5234 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate | HCID 86690079 | 30,2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09326973B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-123710cb3b9642a2a1939182945b1418 |
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| Quellennotiz | uspto-grants-2016_05 |
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