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Methylamine → Tert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate

HRID 2403409
ノート
印刷プレビュー

反応式

HRID 2403409 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][CH:9]1[CH:13]=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:15][NH2:16].[BH4-].[Na+]>CO>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][CH:9]1[CH2:13][NH:16][CH3:15])=[O:7])([CH3:4])([CH3:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6329MethylamineHCID 42278151-Boc-2-FormylpyrrolidineHCID 4311764Sodium borohydride

生成物 1

HCID 53346604Tert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate収率 88.8%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a suspension of 2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (2.68 g) in methanol (30 mL) at room temperature was added a solution of methylamine (831 mg) in methanol (3 mL). The reaction mixture was stirred at room temperature for 72 h and then sodium borohydride (760 mg) and molecular sieves were added. After stirring at room temperature for 2 h, the reaction mixture was filtered and the filtrate reduced in vacuo. The residue was redissolved in dichloromethane (30 mL) and washed with saturated sodium bicarbonate solution (30 mL). The combined organics were washed with brine (30 mL), dried (MgSO4) and reduced in vacuo to give 2-methylaminomethyl-pyrrolidine-1-carboxylic acid tert-butyl ester as a pale yellow oil (2.56 g).

後処理

  1. stirringAfter stirring at room temperature for 2 h
  2. filtrationthe reaction mixture was filtered
  3. dissolutionThe residue was redissolved in dichloromethane (30 mL)
  4. washwashed with saturated sodium bicarbonate solution (30 mL)
  5. washThe combined organics were washed with brine (30 mL)
  6. dry with materialdried (MgSO4)

出典と根拠

ORDレコード
ord-49bf0b221fad4bc8a811fc6ff0269e4c
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08802670B2

反応ノート

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