HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 10200481, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 21994389 | HCID 21994389 | — |
| Product | HCID 10200481 | HCID 10200481 | 89.4% |
Reaction Steps
According to the same procedure as in Example 26, using 3-(3-cyclohexyloxy-4-methoxyanilino)-2-cyclopenten-1-one produced in Example 13(3) instead of 3-(3-cyclopentyloxy-4-methoxyanilino)-2-cyclopenten-1-one, and using benzyl bromide instead of methyl iodide, the title compound (yield 89.4%) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235736B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-49d0d90a004f43149c68a0b4f867b0d3 |
| Source note | uspto-grants-2001_05 |