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3-Hydroxycycloheptanone → Cycloheptane-1,3-dione

HRID 1758164
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HRID 1758164 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 109755023-Hydroxycycloheptanone

생성물 1

HCID 4072367Cycloheptane-1,3-dione수율 58%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

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.

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custom
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
  • 출처 및 근거

    ORD 기록
    ord-56df9c50ed1c4595b051861fc8a361cc
    출처 데이터셋
    uspto-grants-1983_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04371720

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