HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911521Generated: October 30, 2026
(R)-Tert-butyl 4-acetyl-2,2-dimethyloxazolidine-3-carboxylate → HCID 68714982, compound
https://huagongshe.com/reaction/1911521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (R)-Tert-butyl 4-acetyl-2,2-dimethyloxazolidine-3-carboxylate | HCID 10977654 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68714982 | HCID 68714982 | 89% |
Reaction Steps
A solution of (R)-4-acetyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (2.80 g, CAS 167102-63-8) in THF (40 ml) was cooled under an argon atmosphere to 0° C. and treated dropwise with benzylmagnesium chloride solution (1 M in diethylether, 34.5 ml). The reaction mixture was stirred at r.t. overnight, then quenched with saturated aqueous NH4Cl (50 ml) and extracted with EtOAc. The organic layer was washed with H2O and brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (silica gel; gradient: cyclohexane ->cyclohexane/EtOAc 3:1) to give (R)-4-(1-hydroxy-1-methyl-2-phenyl-ethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (3.45 g, 89%) as off-white waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604061B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-b63b63a03c6247b786ea3d647a2914ca |
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| Source note | uspto-grants-2013_12 |
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