HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 21997116, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 10921078 | HCID 10921078 | — |
| Reactant | HCID 21997120 | HCID 21997120 | — |
| Product | HCID 21997116 | HCID 21997116 | — |
Reaction Steps
Allyloxyphenethyl methacrylate, 82% purity, was prepared in the manner of Example 3 from 2-(4-allyloxyphenyl)ethyl alcohol. The starting 2-(4-allyloxyphenyl)ethyl alcohol was prepared by alkylation of the corresponding phenolic alcohol with allyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06231714B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-21e64a67c39e47b2b9d5b84366d65de3 |
| Source note | uspto-grants-2001_05 |