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Lithium borohydride → Benzyl (3S*,4R*)-1-(tert-butoxycarbonyl)-4-formylpyrrolidin-3-ylcarbamate

HRID 456259
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HRID 456259 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:12][C@@H:11]([C:13](OCC)=[O:14])[C@H:10]([NH:18][C:19](=[O:28])[O:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Li+].[BH4-]>C1COCC1.O=[Mn]=O>[C:1]([O:5][C:6]([N:8]1[CH2:12][C@@H:11]([CH:13]=[O:14])[C@H:10]([NH:18][C:19](=[O:28])[O:20][CH2:21][C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

5

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HCID 4148881Lithium borohydrideHCID 701984471-Tert-butyl 3-ethyl (3R,4S)-4-{[(benzyloxy)carbonyl]amino}pyrrolidine-1,3-dicarboxylate

생성물 1

HCID 88205697Benzyl (3S*,4R*)-1-(tert-butoxycarbonyl)-4-formylpyrrolidin-3-ylcarbamate

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 8028Tetrahydrofuran용매

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온도
80 °C

실험 절차

To a solution of benzyl (3S*,4R*)-1-(tert-butoxycarbonyl)-4-(ethoxycarbonyl)pyrrolidin-3-ylcarbamate (4.4 g, 11.2 mmol) in 150 mL THF, LiBH4 (0.74 g, 33.6 mmol) was added and the mixture was stirred at 80° C. for 1.5 hours. The mixture was quenched with H2O, extracted with EtOAc, the combined organic extracts were dried with Na2SO4 and evaporated. The residue was re-dissolved in 300 mL CH2Cl2, activated MnO2 (3.86 g, 56 mmol) was added and the mixture was stirred for 24 hours at room temperature. MnO2 was filtered off through Celite, and the filtrate was evaporated giving the title aldehyde.

후처리

  1. customThe mixture was quenched with H2O
  2. extractionextracted with EtOAc
  3. dry with materialthe combined organic extracts were dried with Na2SO4
  4. customevaporated
  5. dissolutionThe residue was re-dissolved in 300 mL CH2Cl2
  6. stirringthe mixture was stirred for 24 hours at room temperature
  7. filtrationMnO2 was filtered off through Celite
  8. customthe filtrate was evaporated

출처 및 근거

ORD 기록
ord-0577f149cd0344748dc03bd68d7b010d
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08497383B2

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