HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 714271Erstellt: 25. Oktober 2026
Water → (NZ)-N-[1-(4-butoxyphenyl)ethylidene]-2-methylpropane-2-sulfinamide
https://huagongshe.com/reaction/714271
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Ethanone, 1-(4-butoxyphenyl)- | HCID 79814 | — |
| Edukt | Tert-Butanesulfinamide | HCID 3382465 | — |
| Katalysator | HCID 178477244 | HCID 178477244 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (NZ)-N-[1-(4-butoxyphenyl)ethylidene]-2-methylpropane-2-sulfinamide | HCID 89599479 | 87% |
Reaktionsschritte
To a stirred solution of 1-(4-butoxyphenyl)ethanone (3 g, 15.60 mmol) and 2-methylpropane-2-sulfinamide (2.84 g, 23.41 mmol) in THF (50 mL) was added tetraethoxytitanium (8.90 g, 39.0 mmol). The reaction was heated to 70° C. for 3 d. Cold water was added and the reaction was stirred vigorously for 20 min. The mixture was filtered through Celite® and the filtrated was diluted with EtOAc. The organic solution was washed with H2O, brine, dried over MgSO4, filtered and concentrated. The crude product was by silica gel chromatography (220 g silica gel, eluted with EtOAc in hexanes) to yield the desired product (4 g, 87%) as a yellow oil. 1H NMR (500 MHz, CDCl3) δ 7.88 (d, J=8.80 Hz, 2H), 6.91 (d, J=8.80 Hz, 2H), 4.02 (t, J=6.46 Hz, 2H), 2.73 (s, 3H), 1.75-1.83 (m, 2H), 1.46-1.56 (m, 2H), 1.32 (s, 9H), 0.99 (t, J=7.43 Hz, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09187424B1 |
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| Quelldatensatz | uspto-grants-2015_11 |
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| ORD ID | ord-b891d8dd9eb647e0ba02a79e7d75d5f6 |
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| Quellennotiz | uspto-grants-2015_11 |
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