Ammonia → 4-Morpholinecarbothioamide

HRID 2210961Notes

Reaction equation

HRID 2210961 reaction equation
[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]

Participants

5

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-7640f6f9940641bfa971a035c84d3e73
Source dataset
uspto-grants-1995_10
Patent number
US05461067

Reaction notes

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