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Ammonia → 4-Morpholinecarbothioamide

HRID 53936
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 53936
[C:1](C1NC=CN=1)(C1NC=CN=1)=[S:2].[NH:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1.[NH3:19]>C1COCC1>[NH2:19][C:1]([N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1)=[S:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 222AmmoniaHCID 8083Morpholine2×HCID 11412697Thiocarbonyl diimidazole

Produkt 1

HCID 23935444-MorpholinecarbothioamideAusbeute 76 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of 3.35 g (18.8 mmol) of thiocarbonyl diimidazole in 100 ml of THF was treated with 0.82 ml (9.4 mmol) of morpholine. After being stirred at ambient temperature for 3.5 h, an additional 0.82 ml portion of morpholine was added, and stirring was continued. After 6 h, the solution was treated with excess concentrated aqueous ammonia, and stirred overnight. The resulting solution was concentrated in vacuo, taken up in chloroform, separated from the aqueous phase, dried over Na2SO4, and concentrated. Purification of the residue by silica gel chromatography using ethyl acetate provided 1.85 g (76%) of the desired compound, Rf 0.17 (10% methanol in chloroform), as a white solid. 1H NMR (CDCl3) δ 3.76 (m, 4 H), 3.83 (m, 4 H), 5.75 (br, 2 H). Mass spectrum: (M+H)+ =147.

Aufarbeitung

  1. stirringstirring
  2. waitAfter 6 h
  3. stirringstirred overnight
  4. concentrationThe resulting solution was concentrated in vacuo
  5. customseparated from the aqueous phase
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customPurification of the residue by silica gel chromatography

Quellen und Nachweise

ORD-Eintrag
ord-37c5fddb6eed44179c3fbb7830da8477
Quelldatensatz
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05621109

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