HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 131711324, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 31460-31-8 | HCID 1551518 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131711324 | HCID 131711324 | 111.5% |
Reaction Steps
39 g (0.06 mole) of tetrabutylammonium hydroxide solution (40% in water) is added to the suspension of 13.15 g of N-(2,6-dimethylphenyl)-maleamic 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 30.8 g of N-(2,6-dimethylphenyl)-maleamic acid tetrabutylammonium salt in the form of yellow oil, which crystallises on prolonged standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125398 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-079383abb3ae4739995b25145c058950 |
| Source note | uspto-grants-1978_11 |