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Benzaldehyde → (3R,4R)-di-tert-butyl 4-(benzyl(methyl)amino)pyrrolidine-1,3-dicarboxylate

HRID 456347
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HRID 456347 반응식
[NH2:1][C@H:2]1[CH2:6][N:5]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:4][C@H:3]1[C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15].[CH:21](=O)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.[C:29](O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl.CO>[CH2:21]([N:1]([CH3:29])[C@H:2]1[CH2:6][N:5]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:4][C@H:3]1[C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1
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반응물 3

HCID 240BenzaldehydeHCID 5049666Sodium triacetoxyborohydrideHCID 11483050(3R,4R)-di-tert-butyl 4-aminopyrrolidine-1,3-dicarboxylate

생성물 1

HCID 68556735(3R,4R)-di-tert-butyl 4-(benzyl(methyl)amino)pyrrolidine-1,3-dicarboxylate수율 88%

시약·촉매·용매 1

HCID 21226129Dichloromethane methanol용매

실험 절차

To a solution of (3R,4R)-di-tert-butyl 4-aminopyrrolidine-1,3-dicarboxylate (Org. Biomol. Chem. 2004, 2, 2763-2776) (430 mg, 1.5 mmol) in dichloromethane/methanol (18 mL/2 mL) was added benzaldehyde (153 uL, 1.5 mmol) and sodium triacetoxyborohydride (1.89 g, 9.0 mmol). The mixture was stirred overnight and partitioned between ethyl acetate and water. The organic layer was washed with brine, dried with magnesium sulfate, filtered and evaporated. The residue was purified on silica gel eluting with ethyl acetate/hexane (1:3) to give the title compound (495 mg, 88%). MS (ESI+) m/z=377 (M+H)+.

후처리

  1. custompartitioned between ethyl acetate and water
  2. washThe organic layer was washed with brine
  3. dry with materialdried with magnesium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customThe residue was purified on silica gel eluting with ethyl acetate/hexane (1:3)

출처 및 근거

ORD 기록
ord-1495509d5774413d843b4414b9bc7342
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08497275B2

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