Hydrogen Peroxide → 1,4-Dioxaspiro[4.5]decan-8-ylmethanol

HRID 605449Notes

Reaction equation

HRID 605449 reaction equation
B1[CH:6]2[CH2:7][CH2:8][CH2:9][CH:2]1C[CH2:4][CH2:5]2.[OH-:10].[Na+].[OH:12]O.[CH2:14]1[CH2:18][O:17]CC1>>[O:17]1[C:8]2([CH2:7][CH2:6][CH:5]([CH2:4][OH:12])[CH2:2][CH2:9]2)[O:10][CH2:14][CH2:18]1

Participants

5

Procedure

In a reactor under nitrogen atmosphere, 10.6 g of 8-methylene-1,4-dioxaspiro[4.5]decane obtained in the first step was dissolved in 50 mL of THF, and the solution was cooled to 0° C., to which 150 mL of 9-BBN (0.5M, THF solution) was added dropwise. After stirring at room temperature for 48 hours, the reaction mixture was cooled to 0° C., to which 40 mL of a 6M sodium hydroxide aqueous solution was added. The solution was maintained at 0° C., to which a 35% hydrogen peroxide solution was added dropwise. The reaction mixture was washed with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to provide 7.3 g of (1,4-dioxaspiro[4.5]dec-8-yl)methanol.

Workup

  1. additionwas added dropwise
  2. additionwas added
  3. additionwas added dropwise
  4. washThe reaction mixture was washed with a saturated sodium chloride aqueous solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-119b04be5f974480904ca33071a0fca6
Source dataset
uspto-grants-2011_03
Patent number
US07914862B2

Reaction notes

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