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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthanone, 1-(4-butoxyphenyl)-HCID 79814—
EduktTert-ButanesulfinamideHCID 3382465—
KatalysatorHCID 178477244HCID 178477244—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(NZ)-N-[1-(4-butoxyphenyl)ethylidene]-2-methylpropane-2-sulfinamideHCID 8959947987%

Reaktionsbedingungen

Temperatur70 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187424B1
Quelldatensatzuspto-grants-2015_11
ORD IDord-b891d8dd9eb647e0ba02a79e7d75d5f6
Quellennotizuspto-grants-2015_11