HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Phenylenediamine → 3,3-Dimethyloctahydroquinoxalin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,3-Dimethyloctahydroquinoxalin-2(1H)-one | HCID 12886756 | — |
Reaction Steps
5.4 parts of o-phenylene diamine are placed in a flask and ethyl-2-bromoisobutyrate added thereto with ethanol solvent. The reaction mixture is heated and 3,3-dimethyl-3,4-dihydroquinoxalin-2-one is recovered. Upon hydrogenation in the presence of catalyst, 3,3-dimethyl-decahydroquinoxalin-2-one is formed which, when used at 0.5 phr concentration in polypropylene in a manner analogous to that set forth in Example 1A above, provides stabilization for about 2000 hours (see Table I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04466916 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-8127ed53582e49f889eb342eb7b629de |
| Source note | uspto-grants-1984_08 |