Methyl cyanoacetate → 4-(Cyanoacetyl)morpholine

HRID 351453Notes

Reaction equation

HRID 351453 reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[C:7]([CH2:9][C:10](OC)=[O:11])#[N:8]>CC(OC)(C)C>[N:1]1([C:10](=[O:11])[CH2:9][C:7]#[N:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1

Participants

4

Conditions

Temperature
55 °C

Procedure

A nitrogen inerted reactor equipped with reflux condenser, nitrogen inlet and mechanical stirring is charged with morpholine (1.2 mol), methyl cyanoacetate (1.0 mol) and MtBE (52 mL). The homogeneous solution is heated to ca. 55° C. and stirred at that temperature for 12 to 18 hours. MtBE (33 mL) is added over ca. 15 minutes, and the solution is slowly cooled below 50° C. where nucleation becomes evident. Additional MTBE (66 μL) is added over a 1-hour period. During this time, the reaction is allowed to cool to near ambient temperature. After complete MtBE addition, the reaction is cooled with stirring to ca. 0° C. The resulting precipitate is collected via filtration and the cake is washed with additional MtBE (ca. 40 mL). The solid is dried under vacuum at ca. 45° C. to provide 3-morpholin-4-yl-3-oxo-propionitrile (139 g). This material is used in subsequent steps without further purification.

Workup

  1. customA nitrogen inerted reactor equipped
  2. temperaturewith reflux condenser, nitrogen inlet
  3. stirringstirred at that temperature for 12 to 18 hours
  4. additionMtBE (33 mL) is added over ca. 15 minutes
  5. customis slowly cooled below 50° C.
  6. temperatureto cool to near ambient temperature
  7. additionAfter complete MtBE addition
  8. temperaturethe reaction is cooled
  9. stirringwith stirring to ca. 0° C
  10. filtrationThe resulting precipitate is collected via filtration
  11. washthe cake is washed with additional MtBE (ca. 40 mL)
  12. customThe solid is dried under vacuum at ca. 45° C.

Sources & evidence

ORD record
ord-64bdf43cc1f04a579786fe52bf4a94fd
Source dataset
uspto-grants-2007_02
Patent number
US07183408B2

Reaction notes

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