HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445878Generated: October 29, 2026
2-Oxazolidinone → (R)-4-benzyl-3-((R)-3-(4-(benzyloxy)phenyl)-2-methylpropanoyl)oxazolidin-2-one
https://huagongshe.com/reaction/445878
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Oxazolidinone | HCID 73949 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 1-(Benzyloxy)-4-(bromomethyl)benzene | HCID 10492756 | — |
| Reactant | (R)-(-)-4-Benzyl-3-propionyl-2-oxazolidinone | HCID 10966403 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-4-benzyl-3-((R)-3-(4-(benzyloxy)phenyl)-2-methylpropanoyl)oxazolidin-2-one | HCID 59419856 | — |
Reaction Steps
To a solution of (R)-4-benzyl-3-propionyloxazolidin-2-one (17.0 g, 72.8 mmol) in tetrahydrofuran (200 mL) at −78° C. was added sodium bis(trimethylsilyl)amide (80 mL, 79.4 mmol) and stirred for 1 hour. A solution of 1-(benzyloxy)-4-(bromomethyl)benzene (746) (20.0 g, 72.2 mmol) in tetrahydrofuran (50 mL) was added slowly to the oxazolidinone solution at −78° C. and allowed to warm to room temperature overnight. The solvent was removed in vacuo and the residue was dissolved with ethyl acetate. The organic layer was washed with water, brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (20%) to afford (R)-4-benzyl-3-((R)-3-(4-(benzyloxy)phenyl)-2-methylpropanoyl)oxazolidin-2-one (747).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476308B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-799232452a5648729d61a4a15000ca3d |
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| Source note | uspto-grants-2013_07 |
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