Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-Bromovaleryl chloride | HCID 521173 | — |
| Reactant | 4-Benzyl-1,3-oxazolidin-2-one | HCID 559668 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 57612782 | HCID 57612782 | 99.7% |
Reaction Steps
To a solution of S-(−)-4-benzyl-2-oxazolidinone (8.0 g, 45.1 mmol) in THF (75 mL) at −70° C., is added n-BuLi (19.8 mL, 49.6 mmol, 2.5 M in hexane) slowly. After stirring at −70° C. for 1 hour, 5-bromovaleryl chloride (11.7 g, 58.7 mmol) is added dropwise. After stirring at −70° C. for 20 minutes, the cooling bath is removed and the reaction mixture is warmed to 25° C. and stirred for 2 hours. The solution is diluted with 150 mL of ether, and washed with 2×100 mL of water. The combined organic layers is dried over Na2SO4 and concentrated. The crude product is purified by chromatography (hexane/EtOAc:85/15) to give a white solid (15.3 g, 99.7%). (NMR and MS data confirmed, U-3133-51-24).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07989441B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-e5e35b7802a24e7091b22f2f34bfd66f |
|---|
| Source note | uspto-grants-2011_08 |
|---|