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HRID 1009106Erstellt: 26. Oktober 2026

Triethylsilanol → (NE,R)-N-[2-[1-[tert-butyl(dimethyl)silyl]oxycyclopropyl]ethylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1009106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylsilanolHCID 69005—
Edukttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
Edukt2-{1-[(Tert-butyldimethylsilyl)oxy]cyclopropyl}acetaldehydeHCID 86614119—
LösungsmittelDichloromethaneHCID 6344—
Produkt(NE,R)-N-[2-[1-[tert-butyl(dimethyl)silyl]oxycyclopropyl]ethylidene]-2-methylpropane-2-sulfinamideHCID 87349123—

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

To a 1.0 L round bottom flask containing 2-(1-(tert-butyldimethylsilyloxy)cyclopropyl)acetaldehyde (5.00 g, 23.3 mmol) (crude 10.5 g with TESOH, 1H NMR showed about 50/50 sm to impurity) was added DCM (200 mL) and the mixture was allowed to stir at 23° C. for 5 min. At this time, (R)-2-methylpropane-2-sulfinamide (2.83 g, 23.3 mmol) and cupric sulfate anhydrous (2.58 ml, 58.3 mmol) were added and the reaction was allowed to stir for 40 h. The copper salts were removed by celite filtration. The filtrate was concentrated to give a yellow oil that was purified on a 330 g Isco column (5 to 20% EtOAc in hexanes) to afford the title compound as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973047B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-e98deeed756841f9b628db108597f238
Quellennotizuspto-grants-2011_07