HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 10921078, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Tyrosol | HCID 10393 | — |
| Product | HCID 10921078 | HCID 10921078 | 77% |
Reaction Steps
The two-step synthetic procedure of Example 1 was repeated starting with 2-(4-hydroxyphenyl)ethyl alcohol. In this case 1.2 equivalents of allyl bromide was employed in the alkylation step and the intermediate 4-allyloxyphenethyl alcohol was obtained in 77% yield following vacuum distillation (104-112° C. at 0.2 torr). Esterification of the alcohol with methacrylic acid afforded 4-allyloxyphenethyl methacrylate (AOPMA) in 88% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06231714B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-81b6d44d9a534c28af1ea5df49d96430 |
| Source note | uspto-grants-2001_05 |