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1-Aminomethyl-5-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol → 1-methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one

HRID 1936966
ノート
印刷プレビュー

反応式

HRID 1936966 の反応式
N[CH2:2][C:3]1([OH:15])[C:12]2[C:7](=[C:8]([O:13][CH3:14])[CH:9]=[CH:10][CH:11]=2)[CH2:6][CH2:5][CH2:4]1.N([O-])=O.[Na+]>O1CCOCC1.C(O)(=O)C.O.C(OCC)(=O)C>[CH3:14][O:13][C:8]1[C:7]2[CH2:6][CH2:5][CH2:4][C:3](=[O:15])[CH2:2][C:12]=2[CH:11]=[CH:10][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 2

HCID 224629121-Aminomethyl-5-methoxy-1,2,3,4-tetrahydronaphthalen-1-olHCID 23668193Sodium Nitrite

生成物 1

HCID 127282361-methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one収率 52%

試薬・触媒・溶媒 4

HCID 176Acetic Acid溶媒HCID 962Water溶媒2 回HCID 8857
Ethyl Acetate
溶媒
HCID 312751,4-Dioxane溶媒

実験手順

To a solution of 1-aminomethyl-5-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol (26.6 g) in 1,4-dioxane (60 ml), acetic acid (24 ml) and water (210 ml) was added sodium nitrite (9.7 g) in water (60 ml) dropwise at 5° C., and the mixture was stirred at the same temperature for 2.5 hours. The resulting mixture was diluted with ethyl acetate and separated. The organic layer was washed with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was chromatographed (hexane-ethyl acetate) over silica gel to afford 1-methoxy-5,7,8,9-tetrahydro-6H-benzocyclohepten-6-one (12.7 g).

後処理

  1. customseparated
  2. washThe organic layer was washed with saturated aqueous sodium bicarbonate and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customevaporated in vacuo
  5. customThe residue was chromatographed (hexane-ethyl acetate) over silica gel

出典と根拠

ORDレコード
ord-27d80c10d6244a83925f7c7cce729474
出典データセット
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06391915B2

反応ノート

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