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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238572Generated: October 26, 2026

3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)- → HCID 10946477, compound

https://huagongshe.com/reaction/238572

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)-HCID 179824—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
CatalystTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10946477HCID 1094647792.7%

Reaction Steps

To a mixture of (S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (1.0 g, 4.36 mmol), (trifluoromethyl)trimethylsilane (2.0 M solution in THF, 2.6 mL, 5.20 mmol) in THF (10 mL) was added tetrabutylammonium fluoride (1.0 M solution in THF, 0.1 mL, 0.10 mmol) at 0° C. After addition, the mixture was stirred at room temperature for 60 h. Then, tetrabutylammonium fluoride (1.0 M solution in THF, 9 mL, 9.0 mmol) was added and the mixture stirred for another 6 h and subsequently quenched by adding saturated aq. NaHCO3 solution, extracted with EtOAc. The extracts were washed with saturated aq. NaHCO3 solution, water, brine and dried over Na2SO4. Concentration and purification gave (S)-tert-butyl 2,2-dimethyl-4-(2,2,2-trifluoro-1-hydroxyethyl)oxazolidine-3-carboxylate (1.21 g, 92%), which showed a complicated NMR spectrum because of the different comformers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642632B2
Source datasetuspto-grants-2014_02
ORD IDord-93324d6f5b2344c5b14a673db5d4e78e
Source noteuspto-grants-2014_02