HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 22100535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | HCID 11777088 | HCID 11777088 | — |
| Product | HCID 22100535 | HCID 22100535 | — |
Reaction Steps
Next, 4-(1-tert-butoxycarbonylaminocyclobutyl)-2-pyrrolidone is allowed to react with benzyl bromide or benzyl chloride using a base to yield 1-benzyl-4-(1-tert-butoxycarbonylaminocyclobutyl)-2-pyrrolidone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849757 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-64c52dcd682c44d985011e5d0abeb642 |
| Source note | uspto-grants-1998_12 |