HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-phenylmaleamic acid benzyltrimethyl-ammonium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | Maleic acid anilide | HCID 1550938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-phenylmaleamic acid benzyltrimethyl-ammonium salt | HCID 131711323 | 108.1% |
Reaction Steps
48.2 g (0.1 mole) of benzyltrimethylammonium hydroxide solution (34.7% in methanol) is added to 19.1 g (0.1 mole) of N-phenylmaleamic acid in 100 ml of methanol, and the reaction mixture is stirred for one hour at room temperature. The pH-value is adjusted to about 7.0 with acetic acid, and the solvent is removed in vacuo in a rotary evaporator to leave 36.8 g of N-phenylmaleamic acid benzyltrimethyl-ammonium salt in the form of yellow oil, which crystallises after prolonged standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125398 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-ae0d128bcbcc4fb4a9248ecc6adad4e9 |
| Source note | uspto-grants-1978_11 |