HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255791Generated: November 1, 2026
Potassium Hydroxide → 1,1-Dimethylethyl 4-ethenylphenyl carbonate
https://huagongshe.com/reaction/2255791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,1-Dimethylethyl 4-ethenylphenyl carbonate | HCID 93485 | 103.4% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05241098 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-58e30152147a4d05a4deb675ed7b05a3 |
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| Source note | uspto-grants-1993_08 |
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