HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Dimethylaminopyridine → N-(p-chlorophenyl)valine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 6-Phenoxy-2-pyridinemethanol | HCID 12879155 | — |
| Reactant | 3-(4-Chlorophenyl)-4-isopropyloxazolidine-2,5-dione | HCID 13229494 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(p-chlorophenyl)valine | HCID 13796078 | — |
Reaction Steps
To a solution of 3-(4-chlorophenyl)-4-isopropyl-oxazolidine-2,5-dione (336 mg, 1.32 mmol) and dimethylaminopyridine in 5 ml of dry tetrahydrofuran is added a solution of (6-phenoxy-2-pyridyl)methanol (254 mg, 1.26 mmol) in 3 ml of dry tetrahydrofuran. The reaction mixture is stirred for about 20 hours, under dry air, and then diluted with ether followed by washing with saturated aqueous sodium bicarbonate, water and saturated aqueous sodium chloride. After drying over calcium sulfate, solvent is evaporated. The crude product, yellow liquid, is chromatographed on a rotary chromatograph eluting with 15% ether/hexane to give the (6-phenoxy-2-pyridyl)methyl ester of N-(4-chlorophenyl)valine, a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226872 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-daaf4669c68d4fa1a53fb6d4550d01ad |
| Source note | uspto-grants-1980_10 |