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Dicyclopropyl ketone → (R)-N-(dicyclopropylmethylidene)-2-methylpropane-2-sulfinamide

HRID 410497
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 410497
[CH:1]1([C:4]([CH:6]2[CH2:8][CH2:7]2)=O)[CH2:3][CH2:2]1.[CH3:9][C:10]([S@:13]([NH2:15])=[O:14])([CH3:12])[CH3:11]>O1CCCC1.[Cl-].[Na+].O.[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC>[CH:1]1([C:4]([CH:6]2[CH2:8][CH2:7]2)=[N:15][S@@:13]([C:10]([CH3:12])([CH3:11])[CH3:9])=[O:14])[CH2:3][CH2:2]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 70721Dicyclopropyl ketoneHCID 10964479tert-Butylsulfinamide, (R)-(+)-

Produkt 1

HCID 86658247(R)-N-(dicyclopropylmethylidene)-2-methylpropane-2-sulfinamideAusbeute 22,3 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 76524Titanium tetraethoxideKatalysatorHCID 8028TetrahydrofuranLösungsmittel
HCID 57417360
Sodium chloride; water
Lösungsmittel

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

A 20-mL microwave vial containing a solution of dicyclopropyl ketone (0.778 ml, 6.81 mmol), (R)-2-methylpropane-2-sulfinamide (0.825 g, 6.81 mmol), and titanium ethoxide (1.427 ml, 6.81 mmol) in tetrahydrofuran (13.5 mL) under argon was heated in a microwave for 5 minutes at 150° C. and then again at 160° C. for an additional 5 minutes. The reaction mixture was poured into brine (14 mL), the resulting slurry filtered through Celite, and the two resulting layers were separated. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were dried over sodium sulfate, filtered, and concentrated. The crude material was purified by silica gel flash chromatography (10-50% ethyl acetate/hexanes) to afford (R)—N-(dicyclopropylmethylidene)-2-methylpropane-2-sulfinamide (0.325 g, 1.52 mmol, 22% yield). MS ESI: [M+H]+ m/z 214.1.

Aufarbeitung

  1. filtrationthe resulting slurry filtered through Celite
  2. customthe two resulting layers were separated
  3. extractionThe aqueous layer was extracted with ethyl acetate
  4. dry with materialthe combined organic layers were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude material was purified by silica gel flash chromatography (10-50% ethyl acetate/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-16849fc27c7c4977969e3eefe1a336d6
Quelldatensatz
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08759366B2

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