HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethylbutadiene → N-(2,4-pentadienyloxy)-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethylbutadiene | HCID 548848 | — |
| Reactant | N-allyloxy-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine | HCID 11207972 | — |
| Reactant | Tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine | HCID 22182216 | — |
| Product | N-(2,4-pentadienyloxy)-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine | HCID 73988146 | 80% |
Reaction Steps
The compound is prepared in analogy to compound 204 from tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine and 1-brom-2,4-pentadien in 80% yield as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518326B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-9d28527cf9954cc2b5c278a97c1acd60 |
| Source note | uspto-grants-2003_02 |