HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoethene → HCID 68938678, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoethene | HCID 11641 | — |
| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Reactant | 9,10-Dihydro-4-methylene-4H-benzo[4,5]cyclohepta[1,2-b]thiophene | HCID 59769981 | — |
| Product | HCID 68938678 | HCID 68938678 | — |
Reaction Steps
4-Methylene-9,10-dihydro-4H-1-thia-benzo[f]azulene is converted to the vinyl bromide as in Preparation 24 and the vinyl bromide coupled with 3-aminophenylboronic acid using the procedures essentially as described in Example 219.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07411072B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-e581ed6f607d4e3f8a1addfaf5d6cbff |
| Source note | uspto-grants-2008_08 |