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Sodium borohydride → HCID 86695583, 화합물

HRID 1465718
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HRID 1465718 반응식
[O:1]=[C:2]1[CH2:8][C@@H:7]2[N:9]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[C@@H:4]([CH2:5][CH2:6]2)[CH:3]1[C:17]([O:19][CH3:20])=[O:18].[BH4-].[Na+]>CO>[OH:1][CH:2]1[CH2:8][C@@H:7]2[N:9]([C:10]([O:12][C:13]([CH3:14])([CH3:15])[CH3:16])=[O:11])[C@@H:4]([CH2:5][CH2:6]2)[CH:3]1[C:17]([O:19][CH3:20])=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 86695584HCID 86695584, 화합물

생성물 1

HCID 86695583HCID 86695583, 화합물수율 87.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

(1S,5R)-8-Tert-butyl 2-methyl 3-oxo-8-azabicyclo[3.2.1]octane-2,8-dicarboxylate (2 g, 7.04 mmol) was dissolved in MeOH (26 mL), sodium borohydride (280 mg, 7.39 mmol) was added portionwise. The reaction mixture was stirred at room temperature for 1.5 hours. After evaporation, the crude mixture was dissolved in EtOAc, washed with saturated NaHCO3 and water. Dried and concentrate to give 1.75 g of crude product. The crude was carried over the next step without further purification.

후처리

  1. customAfter evaporation
  2. dissolutionthe crude mixture was dissolved in EtOAc
  3. washwashed with saturated NaHCO3 and water
  4. customDried
  5. concentrationconcentrate

출처 및 근거

ORD 기록
ord-109bbaacc1ee40f392468371b3d68deb
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999966B2

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