2,2-Dimethoxypropane → HCID 20077579, compound

HRID 1587797Notes

Reaction equation

HRID 1587797 reaction equation
O.[C:2]1([CH3:12])[CH:7]=[CH:6][C:5]([S:8](O)(=O)=O)=[CH:4]C=1.[F-].[CH2:14]([N+:18](CCCC)(CCCC)CCCC)CCC.[C:31](=O)(O)[O-].[Na+].[CH3:36][O:37][C:38]([O:41]C)([CH3:40])[CH3:39]>C1COCC1>[CH2:2]([CH:7]1[CH2:36][O:37][C:38]([CH3:40])([CH3:39])[O:41][CH:6]1[C:5]1[S:8][CH:14]=[N:18][CH:4]=1)[CH:12]=[CH2:31]

Participants

6

Procedure

p-Toluenesulphonic acid monohydrate (13.4 g) was added to a solution of compound B (20.0 g) in 2,2-dimethoxypropane (100 ml) and the mixture was stirred for 18 hours at ambient temperature. A 1M solution of tetrabutylammonium fluoride in THF (150 ml) was then added and the mixture stirred for a further 15 minutes. The reaction mixture was then neutralised with excess saturated aqueous sodium bicarbonate solution and extracted three times with ethyl acetate. The combined extracts were dried (MgSO4) and concentrated and the residue was purified by column chromatography, eluting with 25% ethyl acetate/hexane (v/v), to give (4RS,5RS)-5-allyl-2,2-dimethyl-4-(5-thiazolyl)-1,3-dioxane (C) (13.0 g; 85% yield) as an oil; NMR: 1.45-1.55(6H,m), 1.6-2.05 and 2.4-2.5(3H,m), 3.68-4.16(2H,m), 4.9-5.1 and 5.5-5.72(4H,m), 7.72 and 7.81(isomers,1H,2s), 8.72 and 8.79(isomers, 1 H,2s).

Workup

  1. stirringthe mixture stirred for a further 15 minutes
  2. extractionextracted three times with ethyl acetate
  3. dry with materialThe combined extracts were dried (MgSO4)
  4. concentrationconcentrated
  5. customthe residue was purified by column chromatography
  6. washeluting with 25% ethyl acetate/hexane (v/v)

Sources & evidence

ORD record
ord-c54c23147ed04bc4bbdfd9d325f27da4
Source dataset
uspto-grants-1993_06
Patent number
US05219874

Reaction notes

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