8-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]decane → 4-(4-Fluorophenyl)cyclohexan-1-one

HRID 1015966Notes

Reaction equation

HRID 1015966 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:17][CH2:16][C:11]3(OCC[O:12]3)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1>C1(C)C=CC=CC=1.C1COCC1.OS(O)(=O)=O.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:9][CH2:10][C:11](=[O:12])[CH2:16][CH2:17]2)=[CH:6][CH:7]=1

Participants

6

Reactant 1

HCID 128344048-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]decane

Product 1

HCID 128343224-(4-Fluorophenyl)cyclohexan-1-oneYield 86%

Reagents, catalysts & solvents 4

HCID 962WaterSolventHCID 1118Sulfuric AcidSolventHCID 1140TolueneSolventHCID 8028TetrahydrofuranSolvent

Procedure

A solution of the intermediate from step B (8.6 g, 36.5 mmol) in toluene (40 mL), THF (20 mL) and 10% H2SO4 in water (25 mL) was stirred at reflux overnight. After cooling to room temperature, the organic layer was separated, washed with brine, dried over MgSO4 and concentrated. Flash chromatography on silica gel eluting with 5% and then 10% EtOAc in hexanes provided the title compound (6.0 g, 86%) as an oil. MS calculated (M+H)+ 193. found 193.

Workup

  1. temperatureat reflux overnight
  2. customthe organic layer was separated
  3. washwashed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-8395ab1e3dc7412187946f5ee9b4a3fc
Source dataset
uspto-grants-2011_07
Patent number
US07985730B2

Reaction notes

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