HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 4-Vinylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Phenylvinyl acetate | HCID 114576 | — |
| Reactant | Dichloromethane cyclohexane | HCID 21916607 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Vinylphenol | HCID 62453 | — |
Reaction Steps
The reaction is based on that described by Corson et al. J Org Chem (1958) 544–549; molar ratios acetoxystyrene:base 1:1.5. The base, KOH in water (30%) was immersed in an ice bath and the acetoxystyrene was added dropwise over 30 mins (all reaction carried under N2; the reaction was TLC monitored (20–80 cyclohexane-dichloromethane) until all acetoxystyrene disappeared, then the pH was brought down to 8 with CO2; the resulting precipitate was filtered and washed with water, then recrystallised from boiling hexane and NMR characterised.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07229836B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-4ecf5b0b53964816bafa471ff6f73896 |
| Source note | uspto-grants-2007_06 |