Benzene → 2-Dimethylaminopyridine

HRID 2049118

Reaktionsgleichung

Reaktionsgleichung von HRID 2049118
[CH3:1][N:2]([CH3:5])[C:3]#[N:4].C#C.[CH:8]1[CH:13]=CC=[CH:10][CH:9]=1>[CH-]1C=CC=C1.[CH-]1C=CC=C1.[Co+2]>[CH3:1][N:2]([C:3]1[CH:10]=[CH:9][CH:8]=[CH:13][N:4]=1)[CH3:5]

Komponenten

5

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

3.1 gm. of cobaltocene (0.016 mole) under nitrogen was dissolved in 44.0 gm. of benzol. The solution mixed with 164 gm. of anhydrous N,N-dimethylcyanamide (2.3 moles). The reaction mixture was saturated with 12 atm. of acetylene at 20° C. in a 1-liter autoclave (with stirring). The reaction mixture was heated to 70° C. Then at the beginning of the exothermal reaction, the heating was carefully increased so that a temperature of 160° C. prevailed in the autoclave. After a drop in pressure in the autoclave to below 12 atm., acetylene was repressed on. After 10 hours of reaction time, the autoclave was cooled down and expansion allowed. As a result of fractional distillation, 238 gm. of 2-(N,N-dimethylamino)-pyridine (boiling point: 92° C., 21 torr) was obtained, after benzol and a small quantity of N,N-dimethylcyanamide had been obtained. The 2-(N,N-dimethylamino)-pyridine had a purity of 99.8 percent--this corresponded to a yield of 84.5 percent.

Aufarbeitung

  1. additionThe solution mixed with 164 gm
  2. customThen at the beginning of the exothermal reaction
  3. temperaturethe heating was carefully increased so that a temperature of 160° C.
  4. customAfter 10 hours of reaction time
  5. temperaturethe autoclave was cooled down
  6. customAs a result of fractional distillation, 238 gm

Quellen und Nachweise

ORD-Eintrag
ord-5d85a4687cd74782a6762d5c68f1f304
Quelldatensatz
uspto-grants-1980_04
Patentnummer
US04196287

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