Formamide → 3-Amino-2,2,4,4-tetramethylthietane

HRID 232336

Reaktionsgleichung

Reaktionsgleichung von HRID 232336
[CH:1]([NH2:3])=O.[CH3:4][C:5]1([CH3:12])[C:8](=O)[C:7](C)([CH3:10])[S:6]1.O.O.O.O.O.O.[Cl-].[Al+3].[Cl-].[Cl-]>O>[NH2:3][CH:1]1[C:7]([CH3:10])([CH3:8])[S:6][C:5]1([CH3:12])[CH3:4]

Komponenten

5

Reaktionsbedingungen

Temperatur
170 °C

Versuchsvorschrift

Formamide (8.0 g, 178 mmol), 2,2,4,4-tetramethyl-3-oxothietane (1.0 g, 6.933 mmol) and aluminum chloride hexahydrate (100 mg) were placed in a Teflon lined Parr bomb and heated at 170° C. for 18 hours. The reaction was then cooled and taken up in water (20 ml). The aqueous solution was extracted with methylene chloride (3×20 ml), the extracts combined and concentrated under reduced pressure. The residue was refluxed with 1N HCl (20 ml) for 4 hours, the reaction cooled and washed with methylene chloride (2×20 ml). It was then brought to pH 14 by addition of 6N sodium hydroxide and extracted with the methylene chloride (3×20 ml). The combined extracts were dried (Na2SO4) and concentrated to give 0.600 g (60%) of title product, verified by its 1H-NMR spectrum.

Aufarbeitung

  1. temperatureThe reaction was then cooled
  2. extractionThe aqueous solution was extracted with methylene chloride (3×20 ml)
  3. concentrationconcentrated under reduced pressure
  4. temperatureThe residue was refluxed with 1N HCl (20 ml) for 4 hours
  5. temperaturethe reaction cooled
  6. washwashed with methylene chloride (2×20 ml)
  7. additionIt was then brought to pH 14 by addition of 6N sodium hydroxide
  8. extractionextracted with the methylene chloride (3×20 ml)
  9. dry with materialThe combined extracts were dried (Na2SO4)
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-d3bd278feb8d4b478b4f07988b4c0c62
Quelldatensatz
uspto-grants-1989_07
Patentnummer
US04851548

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