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5,7-dimethyl-3,4-dihydronaphthalen-1(2H)-one oxime → 5,7-Dimethyl-1,2,3,4-tetrahydronaphthalen-1-amine

HRID 1644118
ノート
印刷プレビュー

反応式

HRID 1644118 の反応式
[CH3:1][C:2]1[CH:11]=[C:10]([CH3:12])[CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][C:7]2=[N:13]O>N.[Ni]>[CH3:1][C:2]1[CH:11]=[C:10]([CH3:12])[CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][CH:7]2[NH2:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 587943195,7-dimethyl-3,4-dihydronaphthalen-1(2H)-one oxime

生成物 1

HCID 111267915,7-Dimethyl-1,2,3,4-tetrahydronaphthalen-1-amine収率 93%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 222Ammonia溶媒

実験手順

5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-amine: A catalytic amount of Raney nickel (slurry in water) was washed with dry MeOH under argon in a round bottom flask. To a solution of the washed Raney Ni in methanolic ammonia (25 mL, 7N), was added 5,7-dimethyl-3,4-dihydronaphthalen-1(2H)-one oxime (example 166b) (420 mg, 2.22 mmol), and the mixture was stirred under a balloon of H2 for 20 hr. Upon completion, the reaction was filtered through celite, the filtrate was concentrated in vacuo, diluted with EtOAC, washed with water and brine, dried over MgSO4, filtered and the solvent was removed under reduced pressure to afford 360 mg of 5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-amine (93%). 1H NMR (500 MHz, CDCl3): δ 1.66-1.83 (m, 4H), 1.96 (m, 2H), 2.19 (s, 3H), 2.28 (s, 3H), 2.55 (m, 1H), 2.66 (m, 1H), 3.97 (m, 1H), 6.88 (s, 1H), 7.09 (s, 1H).

後処理

  1. wash5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-amine: A catalytic amount of Raney nickel (slurry in water) was washed with dry MeOH under argon in a round bottom flask
  2. filtrationUpon completion, the reaction was filtered through celite
  3. concentrationthe filtrate was concentrated in vacuo
  4. additiondiluted with EtOAC
  5. washwashed with water and brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-db3ad710bfa045be946dca0bd898583f
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08124121B2

反応ノート

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