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Sodium borohydride → HCID 67075178, 화합물

HRID 45213
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HRID 45213 반응식
[BH4-].[Na+].[C:3]([O:7][C:8](=[O:26])[NH:9][CH:10]([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1)[CH:11]1[CH2:16][CH2:15][C:14](=[O:17])[CH2:13][CH2:12]1)([CH3:6])([CH3:5])[CH3:4]>CO.C1COCC1>[C:3]([O:7][C:8](=[O:26])[NH:9][CH:10]([CH:11]1[CH2:16][CH2:15][CH:14]([OH:17])[CH2:13][CH2:12]1)[C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1)([CH3:6])([CH3:4])[CH3:5]
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참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 67075403HCID 67075403, 화합물

생성물 1

HCID 67075178HCID 67075178, 화합물

시약·촉매·용매 2

HCID 887Methanol촉매HCID 8028Tetrahydrofuran용매

실험 절차

Sodium borohydride (12 mg, 0.34 mmol) and 2 drops methanol were added to a solution of [(4-methoxy-phenyl)-(4-oxo-cyclohexyl)-methyl]-carbamic acid tert-butyl ester (33, 110 mg) in THF (5 mL). After stirring for 7 hours the reaction was worked up by washing the solution with saturated sodium bicarbonate solution and brine. After drying the organic phase over sodium sulphate, followed by filtration, evaporation gave 101 mg of the desired cis/trans isomer mixture (34) as a colourless solid, which was used directly in the next stage. Rt=1.36, 1.39 min (Method 5). Detected mass: 219.2 (M—C4H8—CO2—H2O+).

후처리

  1. washby washing the solution with saturated sodium bicarbonate solution and brine
  2. dry with materialAfter drying the organic phase over sodium sulphate
  3. filtrationfollowed by filtration, evaporation

출처 및 근거

ORD 기록
ord-5bd95f58e8c946ffaf1f670a019c3d13
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541449B2

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