HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → N-(4-butyl-2-nitrophenyl)-2-(dimethylamino)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide | HCID 21482995 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-butyl-2-nitrophenyl)-2-(dimethylamino)acetamide | HCID 21482988 | — |
Reaction Steps
A suspension of N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide (41 g) in ethanol (200 ml) was treated with a solution of dimethylamine in ethanol (90 ml of 20% w/w). The mixture was refluxed for one hour and the ethanol was evaporated off. Water (100 ml) was added and the mixture extracted with diethyl ether (3 × 200 ml). The extract was dried over magnesium sulphate, filtered and evaporated to give N-(4-n-butyl-2-nitrophenyl)-2-dimethylaminoacetamide as a yellow oil which was used without further purification in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005217 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-a8c4d1c2cf4b458dbbf5cebc50591543 |
| Source note | uspto-grants-1977_01 |