Hydrochloric Acid → 4-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone

HRID 2307099Notes

Reaction equation

HRID 2307099 reaction equation
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:10]=[C:9]([O:11][CH2:12][O:13][CH3:14])[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:24][CH2:23][C:18]2(OCC[O:19]2)[CH2:17][CH2:16]1.Cl.C(=O)(O)[O-].[Na+]>CO>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:10]=[C:9]([O:11][CH2:12][O:13][CH3:14])[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:24][CH2:23][C:18](=[O:19])[CH2:17][CH2:16]1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 121351698-[2,4-Bis(methoxymethoxy)phenyl]-1,4-dioxaspiro[4.5]decane

Product 1

HCID 121351704-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanoneYield 78.9%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A round bottomed flask equipped with magnetic stirrer was charged with 8-[2, 4-bis(methoxymethoxy)phenyl]-1,4-dioxaspiro[4.5]decane (3.20 g 9.47 mmol) and methanol (50 ml). Over a 20 min period, aqueous hydrochloric acid (50 ml, 1.00M) was added to the stirred solution, at room temperature and the reaction mixture stirred for 1.5 hr. Solid sodium bicarbonate was added until the reaction mixture was neutralised and the solvent was removed under reduced pressure. The residue was partitioned between ethyl acetate (30 ml) and water (10 ml), and the aqueous layer was extracted with ethyl acetate (3×20 ml). The combined organic layers were washed with brine (10 ml), dried over magnesium sulfate, filtered and concentrated in vacuo. The crude product was purified via flash column chromatography (SiO2, ethyl acetate/petroleum ether, 1:4, v/v), affording the title compound (2.20 g, 60%) as a white powder. δH(CDCl3) 1.85-1.96 (2H, m), 2.14-2.22 (2H, m), 2.46-2.59 (4H, m), 3.39 (1H, tt), 3.49 (3H, s), 3.52 (3H, s), 5.16 (2H, s), 5.23 (2H, s), 6.67-6.71 (1H, m), 6.85 (1H, m), 7.08 (1H, d).

Workup

  1. customA round bottomed flask equipped with magnetic stirrer
  2. customthe solvent was removed under reduced pressure
  3. customThe residue was partitioned between ethyl acetate (30 ml) and water (10 ml)
  4. extractionthe aqueous layer was extracted with ethyl acetate (3×20 ml)
  5. washThe combined organic layers were washed with brine (10 ml)
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe crude product was purified via flash column chromatography (SiO2, ethyl acetate/petroleum ether, 1:4, v/v)

Sources & evidence

ORD record
ord-6d12543c0e5f4644875a6fc7fada0418
Source dataset
uspto-grants-2004_12
Patent number
US06828460B2

Reaction notes

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