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HCID 12262631、化合物 → 3-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one

HRID 274079
ノート
印刷プレビュー

反応式

HRID 274079 の反応式
N[CH2:2][C:3]1([OH:15])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[CH2:6][CH2:5][CH2:4]1.N([O-])=O.[Na+]>C(O)(=O)C.O>[CH3:14][O:13][C:10]1[CH:9]=[CH:8][C:7]2[CH2:6][CH2:5][CH2:4][C:3](=[O:15])[CH2:2][C:12]=2[CH:11]=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 12262631HCID 12262631、化合物HCID 23668193Sodium Nitrite

生成物 1

HCID 105595743-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one収率 76.8%

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒

実験手順

To a solution of 1-aminomethyl-7-methoxy-1,2,3,4-tetrahydro-1-naphthalenol (27.50 g) in 10% aqueous acetic acid solution (250 ml) was added dropwise a solution of sodium nitrite (10.07 g) in water (61 ml) at 8° C.~9° C. The reaction mixture was stirred for 2 hours at the same temperature. The resulting precipitates were collected by filtration. The precipitates were dissolved in ethyl acetate. The solution was dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography (silica gel, n-hexane:ethyl acetate:chloroform=5:1:3) to give 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-one (19.39 g) as a white powder.

後処理

  1. customThe resulting precipitates
  2. filtrationwere collected by filtration
  3. dissolutionThe precipitates were dissolved in ethyl acetate
  4. dry with materialThe solution was dried over magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was purified by column chromatography (silica gel, n-hexane:ethyl acetate:chloroform=5:1:3)

出典と根拠

ORDレコード
ord-9dda68e7336240aaa16a72cc41678acc
出典データセット
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05387710

反応ノート

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