HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (4R,5S)-4-Methyl-3-((R)-4-methyl-heptanoyl)-5-phenyl-oxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | (4R,5S)-(+)-4-Methyl-5-phenyl-2-oxazolidinone | HCID 2733812 | — |
| Reactant | 4-Methylheptanoic acid, (-)- | HCID 13800370 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4R,5S)-4-Methyl-3-((R)-4-methyl-heptanoyl)-5-phenyl-oxazolidin-2-one | HCID 57160957 | — |
Reaction Steps
To (R)-4-methyl-heptanoic acid (19 g, 0.132 mol) and triethylamine (49.9 g, 0.494 mol) in THF (500 mL) at 0° C. was added trimethylacetylchloride (20 g, 0.17 mol). After 1 hour LiCl (7.1 g, 0.17 mol) was added followed by (4R,5S)-(+)-4-methyl-5-phenyl-2-oxazolidinone) 3 (30 g, 0.17 mol). The mixture was warmed to room temperature and after 16 hours the filtrate was removed by filtration and the solution concentrated under reduced pressure. Flash chromatography (7:1 hexane/EtOAc) gave (4R,5S)-4-methyl-3-((R)-4-methyl-heptanoyl)-5-phenyl-oxazolidin-2-one as an oil. 31.5 g; 79%. [a]D=+5.5 (c 1 in CHCl3). MS, m/z (relative intensity): 304 [M+H, 100%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419981B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-618a4a3542234e029cb50fd22681dc1f |
| Source note | uspto-grants-2008_09 |