Potassium Hydroxide → 1,1-Dimethylethyl 4-ethenylphenyl carbonate

HRID 2255791Notes

Reaction equation

HRID 2255791 reaction equation
[OH-].[K+].[C:3]([O:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])(OC(C)(C)C)=O.C(OC1[CH:29]=[CH:28][C:25]([CH:26]=[CH2:27])=[CH:24][CH:23]=1)(=O)C>CO.C(OCC)(=O)C>[C:14]([O:13][C:11]([O:10][C:3]1[CH:27]=[CH:26][C:25]([CH:28]=[CH2:29])=[CH:24][CH:23]=1)=[O:12])([CH3:15])([CH3:16])[CH3:17]

Participants

6

Reactant 3

HCID 14797Potassium HydroxideHCID 758214-Ethenylphenyl acetateHCID 90495Di-tert-butyl dicarbonate

Product 1

HCID 934851,1-Dimethylethyl 4-ethenylphenyl carbonateYield 103.4%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 8857Ethyl AcetateSolvent

Procedure

A solution of 85 g (1.3 moles) of potassium hydroxide in 161 g of methanol was added in periodic additions along with 229 g (1.0 moles) of di-t-butyl dicarbonate to a stirred solution of 101 g (0.65 moles) of 4-acetoxystyrene in 505 g of ethyl acetate over a period of about 40 minutes. The reagents were added concurrently in approximately equal aliquots while the reaction mixture was kept at 25° C. with an ice bath. After an additional 2 hours of reaction at 25° C., the reaction slurry was washed well with water to remove solids. The volatile components of the organic layer were stripped under vacuum to give 148 g (83% crude yield) of 4-t-butoxycarbonyloxystyrene. Vacuum distillation afforded 87 g (65% yield) of pure product, b.p. 111° C./0.25 mm.

Workup

  1. additionThe reagents were added concurrently in approximately equal aliquots while the reaction mixture
  2. customwas kept at 25° C. with an ice bath
  3. customAfter an additional 2 hours of reaction at 25° C.
  4. washthe reaction slurry was washed well with water
  5. customto remove solids

Sources & evidence

ORD record
ord-58e30152147a4d05a4deb675ed7b05a3
Source dataset
uspto-grants-1993_08
Patent number
US05241098

Reaction notes

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