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Sodium borohydride → HCID 12508669, 화합물

HRID 1633330
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HRID 1633330 반응식
[CH3:1][C:2]12[CH:14]([CH2:15][CH3:16])[N:6]([CH:7]([CH2:12][CH3:13])[NH:8][CH:9]1[CH2:10][CH3:11])[CH:5]([CH2:17][CH3:18])[N:4]=[CH:3]2.[BH4-].[Na+]>[OH-].[Na+].C(O)C>[CH2:3]([C:2]1([CH3:1])[CH:9]([CH2:10][CH3:11])[NH:8][CH:7]([CH2:12][CH3:13])[NH:6][CH:14]1[CH2:15][CH3:16])[NH:4][CH2:5][CH2:17][CH3:18]
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참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 12508656HCID 12508656, 화합물

생성물 1

HCID 12508669HCID 12508669, 화합물수율 90.3%

시약·촉매·용매 2

HCID 14798Sodium Hydroxide촉매HCID 702Ethanol용매

실험 절차

To a mixture of 70 grams of 5-methyl-2,6,8,9-tetraethyl-1,3,7-triazabicyclo (3,3,1) non-3-ene, 0.5 grams of sodium hydroxide, and 190 grams of ethanol was added, with stirring, over a 1/2 hour period 9 grams of sodium borohydride. The mixture was stirred for 20 hours at ambient temperature. The ethanol was removed under diminished pressure and the resulting product was added to water and extracted with ether. The ethereal solution, after drying over anh. MgSO4, was evaporated under diminished pressure to yield 64.2 grams of 5-(2-azapentyl)-5-methyl-2,4,6-triethylhexahydropyrimidine, b.p. 138°-150° C./20 torr.

후처리

  1. additionwas added
  2. customThe ethanol was removed under diminished pressure
  3. additionthe resulting product was added to water
  4. extractionextracted with ether
  5. dry with materialThe ethereal solution, after drying over anh. MgSO4
  6. customwas evaporated under diminished pressure

출처 및 근거

ORD 기록
ord-5641177489ca4d79bf9681b34f631b0a
출처 데이터셋
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04480095

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