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Pyrrolidine → 1-(5-Chloro-2-nitrobenzyl)pyrrolidine

HRID 20282
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반응식

HRID 20282 반응식
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([N+:15]([O-:17])=[O:16])=[C:11]([CH:14]=1)[CH:12]=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([N+:15]([O-:17])=[O:16])=[C:11]([CH:14]=1)[CH2:12][N:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1
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참가 물질

5

반응물 3

HCID 31268PyrrolidineHCID 811235-Chloro-2-nitrobenzaldehydeHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 7833951-(5-Chloro-2-nitrobenzyl)pyrrolidine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Pyrrolidine (4 mL, 48.5 mmol) was added to a solution of 5-chloro-2-nitrobenzaldehyde (6 g, 32.2 mmol) in dichloromethane (150 mL) and the solution was stirred at room temperature for 30 minutes. The solution was then cooled in ice, and sodium triacetoxyborohydride (10.3 g, 48.5 mmol) was added portionwise. Once addition was complete, the reaction was stirred at room temperature for 4 hours. The reaction was washed with sodium carbonate solution, dried over MgSO4 and evaporated under reduced pressure. The residual oil was purified by column chromatography on silica gel using ethyl acetate:pentane (86:14) to afford the title compound as a pale yellow solid, 6.3 g.

후처리

  1. temperatureThe solution was then cooled in ice
  2. additionOnce addition
  3. stirringthe reaction was stirred at room temperature for 4 hours
  4. washThe reaction was washed with sodium carbonate solution
  5. dry with materialdried over MgSO4
  6. customevaporated under reduced pressure
  7. customThe residual oil was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-316009a3be204a12ba994ecef51047aa
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07745630B2

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