Sodium → 4,4,6-Trimethyl-3,4,5,6-tetrahydropyrimidine

HRID 614893

반응식

HRID 614893 반응식
[CH3:1][C:2]1([CH3:9])[CH2:7][C:6]([CH3:8])=[N:5][CH2:4][NH:3]1.[Na]>CO>[CH3:1][C:2]1([CH3:9])[CH2:7][CH:6]([CH3:8])[N:5]=[CH:4][NH:3]1

참가 물질

4

반응물 2

HCID 5360545SodiumHCID 202254014,4,6-Trimethyl-2,3,4,5-tetrahydropyrimidine

생성물 1

HCID 203301244,4,6-Trimethyl-3,4,5,6-tetrahydropyrimidine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a sample of 126 grams of 4,4,6-trimethyl-2,3,4,5-tetrahydropyrimidine in 300 cc. of methanol was added with stirring and cooling over a 2 hr. period 20.8 grams of sodium boronhydride. The mixture was allowed to stand for 17 hrs. The reaction mixture was extracted with chloroform and the chloroform removed under diminished pressure. The remaining product was distilled and the fraction b25 76.5°-77° C. was collected as 108 grams of 4,4,6-trimethyl hexahydropyrimidine. Anal. Calc.ed for C7H16N2 : N, 21.85. Found: N, 21.6 Nuclear magnetic resonance spectrum, solvent CDCl3, δ in ppm; 3.82 s, 2H; 2.87 m, 1H; 1.42 & 1.65, 2d's, 2H; 1.02 d, 3H; 1.08 & 1.13 2s's, 6H; 1.67 s, 2H exchangeable with D2O. A sample of 12.8 grams of 4,4,6-trimethylhexahydropyrimidine and 0.5 grams of 60% nickel catalyst on kieselguhr was heated for 8 hrs. at 185°-187° C. During this time the theoretial amount of hydrogen gas was evolved.

후처리

  1. temperaturecooling over a 2 hr
  2. extractionThe reaction mixture was extracted with chloroform
  3. customthe chloroform removed under diminished pressure
  4. distillationThe remaining product was distilled
  5. customthe fraction b25 76.5°-77° C. was collected as 108 grams of 4,4,6-trimethyl hexahydropyrimidine
  6. custom3.82 s, 2H
  7. custom1.02 d, 3H
  8. custom1.67 s, 2H exchangeable
  9. temperatureA sample of 12.8 grams of 4,4,6-trimethylhexahydropyrimidine and 0.5 grams of 60% nickel catalyst on kieselguhr was heated for 8 hrs
  10. customat 185°-187° C

출처 및 근거

ORD 기록
ord-1d3f6b50d9f642f0af438a9f7f9ad318
출처 데이터셋
uspto-grants-1979_03
특허 번호
US04146714

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