HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → N-benzyloxy-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | N-allyloxy-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine | HCID 11207972 | — |
| Reactant | Tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine | HCID 22182216 | — |
| Product | N-benzyloxy-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine | HCID 22598530 | 92% |
Reaction Steps
The compound is prepared in analogy to compound (204) from tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine and benzylbromide in 92% yield as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06841703B2 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-7be4afed681d4b389306e1f887c1ba30 |
| Source note | uspto-grants-2005_01 |