HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl acrylate → HCID 22154047, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | Acrylate | HCID 25188 | — |
| Reactant | 1-(4-Bromophenyl)ethanol | HCID 95352 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 22154047 | HCID 22154047 | — |
Reaction Steps
p-Bromophenylethanol is first condensed with t-butyl acrylate under conditions of the palladium acetate catalyzed Heck reaction. The resulting acrylate is hydrogenated with palladium on charcoal catalyst to yield t-butyl p-(2-hydroxyethyl)-phenylpropionate, which is converted to the corresponding tosylate by treatment with tosyl chloride in pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04977144 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-30beda62825e43cfa0cfe9436ea85ba8 |
| Source note | uspto-grants-1990_12 |