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1,3-Difluoroacetone → (R)-1-(1,3-difluoropropan-2-yl)pyrrolidin-3-amine

HRID 573156
ノート
印刷プレビュー

反応式

HRID 573156 の反応式
[NH:1]1[CH2:5][CH2:4][C@@H:3]([NH:6]C(=O)OC(C)(C)C)[CH2:2]1.[F:14][CH2:15][C:16](=O)[CH2:17][F:18].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[F:14][CH2:15][CH:16]([N:1]1[CH2:5][CH2:4][C@@H:3]([NH2:6])[CH2:2]1)[CH2:17][F:18]
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 2283971,3-DifluoroacetoneHCID 1514397(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 5049666Sodium triacetoxyborohydride

生成物 1

HCID 67126443(R)-1-(1,3-difluoropropan-2-yl)pyrrolidin-3-amine

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of (R)-tert-butyl pyrrolidin-3-ylcarbamate (0.500 g) and 1,3-difluoropropan-2-one (0.278 g) in dichloromethane (5 mL) was added sodium triacetoxyborohydride (0.853 g). After stirring for 1 hour, the reaction was quenched with saturated NaHCO3 solution (5 mL). The product was extracted into dichloromethane (25 mL), dried over magnesium sulfate, filtered, and concentrated. The resulting crude material was treated with HCl (4.0M in dioxane, 4 mL) and methanol (1 mL) and stirred for 1 hour. The mixture was concentrated to provide the title compound.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customthe reaction was quenched with saturated NaHCO3 solution (5 mL)
  2. extractionThe product was extracted into dichloromethane (25 mL)
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. additionThe resulting crude material was treated with HCl (4.0M in dioxane, 4 mL) and methanol (1 mL)
  7. stirringstirred for 1 hour
  8. concentrationThe mixture was concentrated

出典と根拠

ORDレコード
ord-82df88e44f3a48f0965fc62a96934ead
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09029404B2

反応ノート

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