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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876239Generated: October 30, 2026

Potassium bisulfate → (R)-Benzyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate

https://huagongshe.com/reaction/1876239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 11278709HCID 11278709—
SolventTetrahydrofuranHCID 8028—
Product(R)-Benzyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylateHCID 11414364—

Reaction Steps

A solution of LiALH4 (1 M, 20 mL, 20 mmol) was added dropwise to a cold (−15° C.) solution of (R)-benzyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate (12.2 g, 37.9 mmol) in THF (75 mL). The mixture was stirred for 30 min keeping the temperature below 0° C. A saturated solution of KHSO4 (100 mL) was added slowly to the mixture and it was warmed to room temperature. The mixture was filtered and the solvent was removed to dryness. (R)-benzyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate was obtained as a clear oil (9.161 g, 92% yield) after purification by column chromatography (SiO2, using a mixture of hexane/EtOAc). 1H NMR (CDCl3, 400 mHz, ppm); 1.7 (m, 6H), 4.15 (m, 2H), 4.4 (m, 1H), 5.15, (s, 1H), 5.2 (m, 1H), 7.3 (m, 5H), 9.6 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309593B2
Source datasetuspto-grants-2012_11
ORD IDord-7ec26931123549f19957154e82bd27cb
Source noteuspto-grants-2012_11