HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl bromoacetate → HCID 86585710, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 10612452 | HCID 10612452 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86585710 | HCID 86585710 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of N-hexanoyl-4-(S)-benzyloxazolidin-2-one A-2 (7.3 mmol) in THF at −78° C. is added 1.0 M NaHMDS (8.8 mmol) and the reaction stirred at −78° C. for 1 hour. A solution of methyl bromoacetate (8.8 mmol) in THF is then added dropwise, and the resulting mixture is stirred at −78° C. for 1 hour and then at rt overnight. The reaction is quenched with NH4Cl, concentrated, then suspended in EtOAc and washed with 0.5 N HCl and brine, dried and purified by silica gel chromatography (EtOAc/hexanes) to afford the methyl 3-(R)-(n-butyl)-3-[4-(S)-benzyloxazolidin-2-one-3-ylcarbonyl)propionate (A-3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06987104B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-9e3d21b8fdc54129ab46491dfad36f23 |
| Source note | uspto-grants-2006_01 |