HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → N-(1-phenylethyl)formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | N-(1-phenylethyl)formamide | HCID 97904 | — |
Reaction Steps
In the same manner as in Example 1 except that a mixture of formic acid, ammonium formate and acetophenone was heated with stirring at 160° C. for 6 hours in place of the concurrent addition of acetophenone and formic acid to ammonium formate for 3 hours and keeping the mass after the addition stirred for 3 hours, the reaction and post treatment were carried out to obtain 112 g of crude N-formyl-1-phenylethylamine; the purity: 82.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093851 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-8468a00c9f9943b183cfdddcc8e40cb4 |
| Source note | uspto-grants-2000_07 |