HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenolphthalein → alpha-(2-Fluoro-4-methylphenylamino)isovaleric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenolphthalein | HCID 4764 | — |
| Reactant | 2-Bromoisovaleric acid | HCID 11268 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-4-methylaniline | HCID 67984 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | NaOH ether | HCID 86719931 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | alpha-(2-Fluoro-4-methylphenylamino)isovaleric acid | HCID 20482718 | — |
Reaction Steps
A solution of α-bromoisovaleric acid (8.17 mmole) in methanol is titrated to the phenophthalein end point using sodium methoxide. The solvent is removed by rotoevaporation and then there is added potassium carbonate (1.69 g), 2-fluoro-4-methylaniline (16.38 mmole) and 3 ml HMPT. The reaction is heated at 60° for about 5 hours and then worked up with 5% sodium hydroxide/ether and washed with water (3×). The basic layer is acidified and extracted with ether, washed with water and brine, dried over sodium sulfate and rotoevaporated to yield α-(2-fluoro-4-methylphenylamino)isovaleric acid. (2-Fluoro-4-methylaniline is prepared from 3-fluoro-4-nitrotoluene in a Parr bottle using platinum oxide and hydrogen in ethanol.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04411912 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-b00407b544244c2b81d8fcdf8b143daa |
| Source note | uspto-grants-1983_10 |