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3-Hydroxycycloheptanone → Cycloheptane-1,3-dione

HRID 1762240
Notes
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Reaction equation

HRID 1762240 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 109755023-Hydroxycycloheptanone

Product 1

HCID 4072367Cycloheptane-1,3-dioneYield 58%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

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.

Workup

  1. customTo a 10°-20° C.
  2. customquenched by addition of 12 ml
  3. filtrationThe reaction was filtered through diatomaceous earth
  4. concentrationthe filtrate concentrated on a rotovapor to about 100 ml
  5. additionThe residue was diluted with 300 ml
  6. extractionof saturated sodium chloride and then extracted with six 250 ml
  7. extractionThe combined organic extract
  8. washwas washed with two 100 ml
  9. dry with materialportions of saturated sodium bicarbonate, dried over magnesium sulfate
  10. customevaporated under reduced pressure (aspirator)
  11. customto yield an oil
  12. distillationDistillation of the crude oil
  13. customgave 11.5 g

Sources & evidence

ORD record
ord-817a02c28ee54a85985a33081cc7c055
Source dataset
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04831059

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes