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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
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HRID 2307406 반응식
[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
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참가 물질

5

반응물 2

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

생성물 1

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

시약·촉매·용매 2

HCID 935Nickel촉매HCID 313Hydrochloric Acid용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d967f24a6a3a4a9fa0204c971aadbe38
출처 데이터셋
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06831080B2

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