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1,4-Benzodioxan-6-yl methyl ketone → 1-(2,3-Dihydro-1,4-benzodioxin-6-yl)ethan-1-amine

HRID 2307406
ノート
印刷プレビュー

反応式

HRID 2307406 の反応式
[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([C:11](=O)[CH3:12])=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1.[OH-].[NH4+:15].CO>[Ni].Cl>[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([CH:11]([NH2:15])[CH3:12])=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1
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 2

HCID 761431,4-Benzodioxan-6-yl methyl ketoneHCID 21894508Ammonium hydroxide methanol

生成物 1

HCID 31461111-(2,3-Dihydro-1,4-benzodioxin-6-yl)ethan-1-amine収率 66%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 313Hydrochloric Acid溶媒

実験手順

A mixture of 1-(2,3-dihydro-1,4-benzodioxin-6-yl)acetaldehyde, oxime, (Preparation 5, 10.74 g, 0.0556 mole), and Raney nickel (1 mL) in ammonium hydroxide/methanol (20 mL/200 mL) was hydrogenated (H2, 50 psi) for 48 hours. The reaction mixture was filtered through Celite and the resultant filtrate was concentrated in vacuo. The residual oil obtained was diluted with HCl (1N). The aqueous layer was washed with EtOAc (1×250 mL). The aqueous layer was then made basic with NaOH (1N), and extracted with EtOAc (3×200 mL). The combined organic layers were dried over anhydrous magnesium sulfate, filtered and the resultant filtrate was concentrated in vacuo to provide the title product (7.1 g, 66%) as a clear oil.

後処理

  1. customfor 48 hours
  2. filtrationThe reaction mixture was filtered through Celite
  3. concentrationthe resultant filtrate was concentrated in vacuo
  4. customThe residual oil obtained
  5. washThe aqueous layer was washed with EtOAc (1×250 mL)
  6. extractionextracted with EtOAc (3×200 mL)
  7. dry with materialThe combined organic layers were dried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationthe resultant filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-d967f24a6a3a4a9fa0204c971aadbe38
出典データセット
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06831080B2

反応ノート

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