Sulfuric Acid → 4-(Azetidin-3-yl)morpholine

HRID 478927Notes

Reaction equation

HRID 478927 reaction equation
[N:1]12[CH2:4][CH:3]1[CH2:2]2.Br.BrC(CBr)CN.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.S(=O)(=O)(O)O.[OH-].[Ca+2].[OH-]>C(O)C.O>[NH:1]1[CH2:4][CH:3]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)[CH2:2]1

Participants

8

Procedure

A solution of 1-azabicyclo[ 1.1.0]butane, prepared from 2,3-dibromopropylamine hydrobromide (58.8 mmol) according to a known procedure described in Tetrahedron Lett. 40: 3761-64 (1999), was slowly added to a solution of morpholine (15.7 ml; 180 mmol) and sulfuric acid (3.3 g of 96% soln.) in anhydrous non-denaturated ethanol (250 ml) at 0° C. The reaction mixture was stirred on ice bath for 30 min., then at room temperature for 8 h. Calcium hydroxide (5.5 g) and 100 ml of water was added and the obtained slurry was stirred for 1 h and then filtered through a pad of cellite. The filtrate was concentrated and distilled at reduced pressure (20 mm Hg) to remove water and an excess of morpholine. The distillation residue was re-distilled at high vacuum using a Kugelrohr apparatus to obtain a pure 4-(azetidin-3-yl)morpholine in 33% yield (2.759 g) as a colorless oily liquid.

Workup

  1. waitat room temperature for 8 h
  2. stirringthe obtained slurry was stirred for 1 h
  3. filtrationfiltered through a pad of cellite
  4. concentrationThe filtrate was concentrated
  5. distillationdistilled at reduced pressure (20 mm Hg)
  6. customto remove water
  7. distillationThe distillation residue was re-distilled at high vacuum

Sources & evidence

ORD record
ord-be81a1c16ec04e85a49f85f07b8447ff
Source dataset
uspto-grants-2003_11
Patent number
US06642232B2

Reaction notes

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