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3-Hydroxycycloheptanone → Cycloheptane-1,3-dione

HRID 1758164
ノート
印刷プレビュー

反応式

HRID 1758164 の反応式
[OH:1][CH:2]1[CH2:8][CH2:7][CH2:6][CH2:5][C:4](=[O:9])[CH2:3]1>CC(C)=O>[C:4]1(=[O:9])[CH2:5][CH2:6][CH2:7][CH2:8][C:2](=[O:1])[CH2:3]1
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 109755023-Hydroxycycloheptanone

生成物 1

HCID 4072367Cycloheptane-1,3-dione収率 58%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a 10°-20° C. solution of 20 g. (0.156 mole) of 3-hydroxycycloheptanone in 700 ml. of acetone was slowly added 54.9 ml. of 2.67 M Jone's reagent (0.146 mole). The mixture was stirred 15 minutes and then quenched by addition of 12 ml. of isopropanol. The reaction was filtered through diatomaceous earth and the filtrate concentrated on a rotovapor to about 100 ml. The residue was diluted with 300 ml. of saturated sodium chloride and then extracted with six 250 ml. portions of ether. The combined organic extract was washed with two 100 ml. portions of saturated sodium bicarbonate, dried over magnesium sulfate and evaporated under reduced pressure (aspirator) to yield an oil. Distillation of the crude oil gave 11.5 g. (58%) of the title compound as an oil.

後処理

  1. custom
このページの内容参加物実験手順後処理出典と根拠反応ノート
To a 10°-20° C.
  • customquenched by addition of 12 ml
  • filtrationThe reaction was filtered through diatomaceous earth
  • concentrationthe filtrate concentrated on a rotovapor to about 100 ml
  • additionThe residue was diluted with 300 ml
  • extractionof saturated sodium chloride and then extracted with six 250 ml
  • extractionThe combined organic extract
  • washwas washed with two 100 ml
  • dry with materialportions of saturated sodium bicarbonate, dried over magnesium sulfate
  • customevaporated under reduced pressure (aspirator)
  • customto yield an oil
  • distillationDistillation of the crude oil
  • customgave 11.5 g
  • 出典と根拠

    ORDレコード
    ord-56df9c50ed1c4595b051861fc8a361cc
    出典データセット
    uspto-grants-1983_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04371720

    反応ノート

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