HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-(Aminocarbonyl)benzeneacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-(4-cyanophenyl)acetate | HCID 279718 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-(Aminocarbonyl)benzeneacetic acid | HCID 14180950 | — |
Reaction Steps
A mixture of ethyl 4-cyanobenzeneacetate (1.9 g) and freshly ground KOH (2.8 g) in 2-methylpropan-2-ol (20 ml) was heated under gentle reflux for 20 min. The resulting mixture was cooled, diluted with 50% saturated NaCl solution (50 ml), washed with CHCl3 (4×50 ml), and acidified with 2M hydrochloric acid (25 ml) to precipitate the title compound (1.65 g) as a fine white solid m.p. 226°-227°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855314 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-9bfbdf1916454db791a95e92244874ee |
| Source note | uspto-grants-1989_08 |