Ammonia → 2-(3-Cyanopropyl)-4-dimethylaminomethylpyridine

HRID 365001

반응식

HRID 365001 반응식
S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+].[C:13]([CH2:15][CH2:16][CH2:17][C:18](O)=O)#[N:14].[CH3:21][N:22]([CH2:24][C:25]1[CH:30]=C[N:28]=[CH:27][CH:26]=1)[CH3:23].S(=O)(=O)(O)O.N>O.[N+]([O-])([O-])=O.[Ag+]>[C:13]([CH2:15][CH2:16][CH2:17][C:18]1[CH:30]=[C:25]([CH2:24][N:22]([CH3:23])[CH3:21])[CH:26]=[CH:27][N:28]=1)#[N:14]

참가 물질

8

반응물 5

HCID 222AmmoniaHCID 1118Sulfuric AcidHCID 382394-Cyanobutanoic acidHCID 62648Ammonium PersulfateHCID 2649464-pyridinemethanamine, N,N-dimethyl-

생성물 1

HCID 132926072-(3-Cyanopropyl)-4-dimethylaminomethylpyridine수율 36.9%

시약·촉매·용매 2

HCID 24470Silver Nitrate촉매HCID 962Water용매3회

실험 절차

Ammonium persulphate (54.8 g) in water (150 ml) and 4-cyanobutyric acid (68 g) in water (300 ml) were added separately and simultaneously over 30 minutes to a mixture of 4-dimethylaminomethylpyridine (16.32 g), silver nitrate (4 g), water (200 ml) and concentrated sulphuric acid (25 ml) stirred at 80°. The reaction mixture was stirred at 80° for 1.5 hours, cooled, poured onto crushed ice (400 g) and aqueous ammonia (28% w/w, 200 ml). The solution was extracted with chloroform (900 ml) and the chloroform extracts were washed with dilute sodium hydroxide, dried over magnesium sulphate, and concentrated in vacuo to give 2-(3-cyanopropyl)-4-dimethylaminomethylpyridine (9 g) as a clear oil b.p. 110°-112°/0.1 mm Hg.

후처리

  1. stirringThe reaction mixture was stirred at 80° for 1.5 hours
  2. temperaturecooled
  3. additionpoured
  4. extractionThe solution was extracted with chloroform (900 ml)
  5. washthe chloroform extracts were washed with dilute sodium hydroxide
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-34b2a60254b248fa9b4b6586d976eb46
출처 데이터셋
uspto-grants-1986_08
특허 번호
US04607107

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