HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → N-tert-Butyl-a-phenylnitrone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | N-(1,1-Dimethylethyl)benzenemethanamine | HCID 76908 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-tert-Butyl-a-phenylnitrone | HCID 4390 | — |
Reaction Steps
Following the general procedure of Example 1, N-benzyl-N-tert-butylamine is oxidized using a solution of 3-chloroperoxybenzoic acid dissolved in methylene chloride to give N-tert-butyl-alpha-phenyl nitrone as a white solid melting at 70°-72° C. This is the nitrone described in Japanese Sho No. 59-11345.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04898901 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-4cea29d3563046168c242b9deb9efc7b |
| Source note | uspto-grants-1990_02 |