HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 10294599, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 68464430 | HCID 68464430 | — |
| Product | HCID 10294599 | HCID 10294599 | 92.3% |
Reaction Steps
According to the same procedure as in Example 26, using 3-[3-[(1RS,2RS,4SR)-bicyclo[2.2.1]hept-2-yloxy]-4-methoxyanilino]2-cyclopenten-1-one produced in Example 8(3) instead of 3-(3-cyclopentyloxy-4-methoxyanilino)-2-cyclopenten-1-one, and using benzyl bromide instead of methyl iodide, the title compound (yield 92.3%) was obtained as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235736B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-b1bf9d6678ea49eaa22c43ed08aa35bb |
| Source note | uspto-grants-2001_05 |