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8-Oxabicyclo[5.1.0]octan-2-one → 3-Hydroxycycloheptanone

HRID 1762239
Notes
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Reaction equation

HRID 1762239 reaction equation
[CH:1]12[O:8][CH:7]1[CH2:6][CH2:5][CH2:4][CH2:3][C:2]2=[O:9]>O1CCCC1>[OH:9][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6][C:7](=[O:8])[CH2:1]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 156197338-Oxabicyclo[5.1.0]octan-2-one

Product 1

HCID 109755023-HydroxycycloheptanoneYield 97%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a 25° C. solution of 45.9 g. (0.364 mole) of 8-oxabicyclo[5.l.0]octan-2-one in 950 ml. of 10% aqueous tetrahydrofuran was added 39.7 g. (1.47 mmoles) of aluminum amalgam. (The aluminum amalgam was prepared by 15-30 second successive washing of small pieces of aluminum foil with 2N sodium hydroxide, distilled water, 0.5% mercuric chloride, distilled water, 2N sodium hydroxide, distilled water, 0.5% mercuric chloride, distilled water, ethanol and ether.) The mixture was stirred for 2 hours, then filtered through diatomaceous earth. The filtrate was evaporated on a rotovapor, the residue saturated with solid sodium chloride and extracted with three 500 ml. portions of ether. The ether extract was dried over magnesium sulfate and evaporated to yield 45 g. (97%) of the title compound as an oil.

Workup

  1. customTo a 25° C.
  2. washsuccessive washing of small pieces of aluminum foil with 2N sodium hydroxide
  3. distillationdistilled water, 0.5% mercuric chloride
  4. distillationdistilled water, 2N sodium hydroxide
  5. distillationdistilled water, 0.5% mercuric chloride
  6. distillationdistilled water, ethanol and ether
  7. filtrationfiltered through diatomaceous earth
  8. customThe filtrate was evaporated on a rotovapor
  9. extractionthe residue saturated with solid sodium chloride and extracted with three 500 ml
  10. extractionThe ether extract
  11. dry with materialwas dried over magnesium sulfate
  12. customevaporated
  13. customto yield 45 g

Sources & evidence

ORD record
ord-75b3ea64959a403bb34bfafd5ab39869
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