Hydrochloric Acid → (S)-oxiranylmethyl methanesulfonamide

HRID 12379

Reaktionsgleichung

Reaktionsgleichung von HRID 12379
[CH3:1][S:2]([NH2:5])(=[O:4])=[O:3].[OH-].[Na+].Cl[CH2:9][C@@H:10]1[CH2:12][O:11]1.Cl>O>[O:11]1[CH2:12][C@@H:10]1[CH2:9][CH2:1][S:2]([NH2:5])(=[O:4])=[O:3]

Komponenten

6

Versuchsvorschrift

To a cold solution of methanesulfonamide (10 g, 0.105 mol) in water (100 mL) in an ice bath was added sodium hydroxide as pellets (8.4 g, 0.21 mol) and then (S)-2-chloromethyloxirane (12.4 g, 0.158 mol). The mixture was stirred at the same temperature for 2 h, and at room temperature for 12 h and then concentrated hydrochloric acid (18 mL) was added. The product was isolated by extracting the aqueous layer with dichloromethane (2×300 mL). The organic layer was dried over MgSO4 and then evaporated to dryness, yielding a colorless liquid (2.5 g), which was used directly in the next step.

Aufarbeitung

  1. waitat room temperature for 12 h
  2. customThe product was isolated
  3. extractionby extracting the aqueous layer with dichloromethane (2×300 mL)
  4. dry with materialThe organic layer was dried over MgSO4
  5. customevaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-7d46aa2551e64e31b61c95a914fb29be
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07728006B2

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