HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-bromomethyl-2,4-dichloro-N-methyl-N-(phthalimidoacetyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile) | HCID 85867 | — |
| Reactant | 2,6-dichloro-3-[N-(phthalimidoacetyl)-N-methylamino]toluene | HCID 22113013 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromomethyl-2,4-dichloro-N-methyl-N-(phthalimidoacetyl)aniline | HCID 22113338 | 27.8% |
Reaction Steps
A mixture of 2,6-dichloro-3-[N-(phthalimidoacetyl)-N-methylamino]toluene (303 mg), N-bromosuccinimide (150 mg), 2,2'-azobis-(2,4-dimethyl-4-methoxyvaleronitrile) (30 mg) and dichloromethane (6 ml) was heated under reflux for 5 hours. N-Bromosuccinimide (75 mg) was added therein and the mixture was heated under reflux for additional 3 hours. The reaction mixture was washed with saturated sodium bicarbonate solution twice and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was crystallized from diethyl ether to give 3-bromomethyl-2,4-dichloro-N-methyl-N-(phthalimidoacetyl)aniline (102 mg) as crystals. mp: 211° C. (dec.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922711 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-0dea4617883b498bbc4be403d81c099a |
| Source note | uspto-grants-1999_07 |