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Sodium borohydride → 1-[4-Hydroxy-4-(4-t-butylphenyl)butyl]imidazole

HRID 463281
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HRID 463281 반응식
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11](=[O:20])[CH2:12][CH2:13][CH2:14][N:15]2[CH:19]=[CH:18][N:17]=[CH:16]2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[BH4-].[Na+]>CO>[OH:20][CH:11]([C:8]1[CH:7]=[CH:6][C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])=[CH:10][CH:9]=1)[CH2:12][CH2:13][CH2:14][N:15]1[CH:19]=[CH:18][N:17]=[CH:16]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 202824961-[4-(4-t-Butylphenyl)butan-4-onyl]imidazole

생성물 1

HCID 134573631-[4-Hydroxy-4-(4-t-butylphenyl)butyl]imidazole

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a 0° C. solution of 5.0 g of the above ketone in 150 ml. of anhydrous methanol was added excess sodium borohydride and the mixture stirred for one hour. After removal of the solvent, a small quantity of water was added and the mixture was extracted with ethyl acetate. The combined extracts were dried over magnesium sulfate and evaporated to afford 1-[4-hydroxy-4-(4-t-butylphenyl)butyl]imidazole, which was converted to the oxalate salt and recrystallized from ethyl acetate/ethanol, m.p. 205°-207° C.(foaming).

후처리

  1. customTo a 0° C.
  2. customAfter removal of the solvent
  3. additiona small quantity of water was added
  4. extractionthe mixture was extracted with ethyl acetate
  5. dry with materialThe combined extracts were dried over magnesium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-ac368a735b4f46a5a7d9f55a361b33df
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04518607

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