HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-(2,6-dimethylphenyl)valine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2,6-Dimethylaniline | HCID 6896 | — |
| Reactant | m-Phenoxybenzyl alpha-bromoisovalerate | HCID 13229492 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | N-(2,6-dimethylphenyl)valine | HCID 15383894 | — |
Reaction Steps
To m-phenoxybenzyl α-bromoisovalerate (2 g, 0.0055 mole), 24°, is added 2,6-dimethylaniline (3.33 g, 0.0275 mole) followed by a catalytic amount of potassium iodide (20 mg). The reaction mixture is heated at about 120° for 48 hours, and then poured into ice-water (20 ml) and 2 N sulfuric acid (10 ml) and extracted with ether (3×30 ml). The combined ether extracts are washed with water (2×20 ml) until neutral and with brine (10 ml) followed by drying over calcium sulfate. The reaction product is concentrated under vacuum and isolated by preparative TLC to give m-phenoxybenzyl ester of N-(2,6-dimethylphenyl)valine. MS m/e 403.2 (M+, 7.5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243819 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-597a0fd6ef044e7598ceb2511d1e6afa |
| Source note | uspto-grants-1981_01 |