Hydrochloric Acid → 2-(Isopropylsulfonyl)ethanamine

HRID 585603

Reaktionsgleichung

Reaktionsgleichung von HRID 585603
[CH:1]([S:4]([CH2:7][C:8]#[N:9])(=[O:6])=[O:5])([CH3:3])[CH3:2].CSC.B.Cl>C1COCC1>[CH:1]([S:4]([CH2:7][CH2:8][NH2:9])(=[O:6])=[O:5])([CH3:3])[CH3:2]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 27785302-(Isopropylsulfonyl)acetonitrileHCID 12423031(Dimethyl sulfide)trihydroboron

Produkt 1

HCID 220177492-(Isopropylsulfonyl)ethanamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Prepared according to Procedure K. 2-iso-Propylsulfonylacetonitrile (0.50 g, 3.39 mmol) was dissolved in THF and warmed to reflux under N2. Borane dimethylsulfide (2M, 1.7 mL, 3.39 mmol) was added dropwise and the reaction was stirred for an additional 40 minutes at reflux. After cooling the reaction to rt, HCl (2 M in MeOH) was added to the reaction slowly due to gas evolution. The volatiles were removed and frexh methanol was added to the resulting residue. Again, the volatiles were removed and the resulting residue was taken up in CH2Cl2 (25 mL) and washed with saturated potassium carbonate (aqueous). The organic layer was dried over sodium sulfate and the volatiles were removed to afford the title compound. GC-MS m/z 152 (MH+).

Aufarbeitung

  1. customPrepared
  2. temperaturewarmed
  3. temperatureto reflux under N2
  4. temperatureat reflux
  5. temperatureAfter cooling
  6. customthe reaction to rt
  7. customThe volatiles were removed
  8. additionfrexh methanol was added to the resulting residue
  9. customAgain, the volatiles were removed
  10. washwashed with saturated potassium carbonate (aqueous)
  11. dry with materialThe organic layer was dried over sodium sulfate
  12. customthe volatiles were removed

Quellen und Nachweise

ORD-Eintrag
ord-899de2b1e68b497bb70e297bf99269c9
Quelldatensatz
uspto-grants-2005_08
Patentnummer
US06933299B1

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