HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibenzylamine → 5-((Bis(benzyl)amino)acetyl)salicylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | 5-(Bromoacetyl)salicylamide | HCID 198556 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 5-((Bis(benzyl)amino)acetyl)salicylamide | HCID 121727 | 45% |
Reaction Steps
5-Bromoacetyl salicylamide (515 g) was added to a stirred solution of dibenzylamine (750 g) in ethyl methyl ketone (3.0 l). The mixture was heated at reflux for one hour and the dibenzylamine hydrobromide was filtered and dried. The filtrate was allowed to cool, when the crude product crystallised. This was filtered off, dried, and recrystallised from ethyl acetate, (5 l), to give 5-(N,N-dibenzylglycyl)salicylamide as an off-white solid (336 g), m.p. 168°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101579 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-8be136d62c0548a1be788f742b37722c |
| Source note | uspto-grants-1978_07 |