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Isoxepac → 2-(6,11-Dihydrodibenz[b,e]oxepin-2-yl)ethanol

HRID 357259
ノート
印刷プレビュー

反応式

HRID 357259 の反応式
O=[C:2]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[CH2:6][O:5][C:4]2[CH:13]=[CH:14][C:15]([CH2:17][C:18](O)=[O:19])=[CH:16][C:3]1=2>O1CCCC1>[CH:16]1[C:3]2[CH2:2][C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=3[CH2:6][O:5][C:4]=2[CH:13]=[CH:14][C:15]=1[CH2:17][CH2:18][OH:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 41448Isoxepac

生成物 1

HCID 107287482-(6,11-Dihydrodibenz[b,e]oxepin-2-yl)ethanol収率 15.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 6,11-dihydro-11-oxodibenz[b,e]oxepin-2-acetic acid (100 g) in 450 ml dry tetrahydrofuran (THF) at -5° C. was treated with a 1M solution of boran-THF complex (373 ml in THF) under a nitrogen blanket. After stirring at ambient temperature for 72 hours, the reaction was quenched with methanol then diluted with water. Evaporation of the organic phase left an oily biphase which was basified with saturated sodium bicarbonate and extracted into dichloromethane. The organic phase was dried and evaporated to an oil which was purified by flash chromatography to give 14 g of 2-(6,11-dihydrodibenz[b,e]oxepin-2-yl)ethanol as an oil.

後処理

  • customthe reaction was quenched with methanol
  • additionthen diluted with water
  • customEvaporation of the organic phase
  • waitleft an oily biphase which
  • extractionextracted into dichloromethane
  • customThe organic phase was dried
  • customevaporated to an oil which
  • customwas purified by flash chromatography
  • 出典と根拠

    ORDレコード
    ord-177df3b30ccc470ea6504ea2584e3ab5
    出典データセット
    uspto-grants-1998_11
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05840749

    反応ノート

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