Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413985Generated: October 28, 2026

Formaldehyde → (4S)-N-Boc-4-phenylmethyloxazolidin-5-one

https://huagongshe.com/reaction/413985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantL-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
CatalystBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventTolueneHCID 1140—
Product(4S)-N-Boc-4-phenylmethyloxazolidin-5-oneHCID 1148279972.2%

Reaction Steps

Tert-butoxycarbonyl-L-phenylalanine (20.00 g), paraformaldehyde (6.04 g) and pyridinium p-toluenesulfonate (0.95 g) were added to toluene (200 ml), and they were stirred under heating and reflux for 30 minutes. The reaction mixture was cooled to room temperature and washed with a saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The obtained toluene layer was dried over anhydrous sodium sulfate and then sodium sulfate was removed. The solvent was evaporated under reduced pressure. The concentrated solution was cooled to room temperature to crystallize the product. The crystals were separated and dried to obtain intended (4S)-N-tert-butoxycarbonyl-4-phenylmethyloxazolidin-5-one (15.10 g) (yield: 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06570039B2
Source datasetuspto-grants-2003_05
ORD IDord-481d92e92afd4807b2ac005afe70c119
Source noteuspto-grants-2003_05