HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → N-phenylvaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | alpha-Cyano-m-phenoxybenzyl alpha-bromoisovalerate | HCID 13705788 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | N-phenylvaline | HCID 10867191 | — |
Reaction Steps
To m-phenoxy-α-cyanobenzyl α-bromoisovalerate (2.0 g, 0.0052 mole) in 4 ml of HMPT, at 24°, is added aniline (1.5 g, 0.016 mole) and potassium iodide (21 mg). The reaction is stirred at 65° for 90 hours and then cooled and poured into ice-water (20 ml) plus 2 N sulfuric acid (10 ml). The reaction is worked up as in Example 4 and purified by preparative TLC to give the m-phenoxy-α-cyanobenzyl ester of N-phenylvaline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04411912 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-0c86d464fa1e4e308dfb5a751f11cc6f |
| Source note | uspto-grants-1983_10 |