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Thallous nitrate → 3-methoxy-1,2,3,4-tetrahydro-5H-benzocyclohepten-6-one

HRID 274048
ノート
印刷プレビュー

反応式

HRID 274048 の反応式
[N+]([O-])([O-])=[O:2].[Tl+].[CH2:6]=[C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([O:17][CH3:18])[CH:15]=2)[CH2:10][CH2:9][CH2:8]1>CO.C(Cl)(Cl)Cl>[CH3:18][O:17][CH:14]1[CH2:13][CH2:12][C:11]2=[CH:10][CH:9]=[CH:8][C:6](=[O:2])[CH2:7][CH:16]2[CH2:15]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 24937Thallous nitrateHCID 109650271-Methylene-7-methoxy-1,2,3,4-tetrahydronaphthalene

生成物 1

HCID 676857843-methoxy-1,2,3,4-tetrahydro-5H-benzocyclohepten-6-one収率 70.7%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回HCID 6212Chloroform溶媒

実験手順

To a solution of thallium nitrate (2.4 g) in methanol (24 ml) was added 1-methylene-7-methoxy-1,2,3,4-tetrahydronaphthalene (1.0 g) in methanol (7 ml) in one portion. The mixture was stirred for 1 minute and diluted with chloroform (24 ml). The resulting precipitate was filtered off and the filtrate was washed with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by column chromatography on silica gel (elution; 8:1, n-hexane-ethyl acetate) to give 3-methoxy-1,2,3,4-tetrahydro-5H-benzocyclohepten-6-one (0.78 g).

後処理

  1. filtrationThe resulting precipitate was filtered off
  2. washthe filtrate was washed with saturated aqueous sodium bicarbonate and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography on silica gel (elution; 8:1, n-hexane-ethyl acetate)

出典と根拠

ORDレコード
ord-5c6816d4a0254c81bc22b5e2cf0e7d37
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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