HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464488Generated: October 30, 2026
Potassium Hydroxide → 1,1-Dimethylethyl 4-ethenylphenyl carbonate
https://huagongshe.com/reaction/1464488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Catalyst | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,1-Dimethylethyl 4-ethenylphenyl carbonate | HCID 93485 | 64% |
Reaction Steps
A solution comprising 0.49 grams potassium hydroxide, 40 grams of 4-acetoxystyrene, and 100 grams of absolute ethanol was refluxed for 4 hours. The reaction solution was cooled to 28° C. and 13 grams of potassium hydroxide pellets were added over a period of 10 minutes. After an additional 30 minutes of reaction, 64 grams di-tertiary-butyl-dicarbonate was charged portionwise over 20 minutes and the reaction was stirred for an additional hour at 28° C. After aqueous washing, the reaction product was extracted with ethyl acetate. The ethyl acetate was stripped from the extraction mixture on a rotary evaporator and the residual oil was charged with 0.07 grams phenothiazine. Distillation at 0.1 Mm Hg gave 34.2 grams (64%) 4-tertiary-butoxycarbonyloxystyrene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05304690 |
|---|
| Source dataset | uspto-grants-1994_04 |
|---|
| ORD ID | ord-2e1ed0c5531a4b269cef5768c3b22de1 |
|---|
| Source note | uspto-grants-1994_04 |
|---|