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

HRID 419853

反応式

HRID 419853 の反応式
[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

参加物

5

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-4d36990dc3cd4d02b52bfdff2406ea4c
出典データセット
uspto-grants-2012_01
特許番号
US08093400B2

関連ノート

読み込み中…