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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538919Generated: November 1, 2026

Methanol → (S)-4-Methoxymethyl-oxazolidin-2-one

https://huagongshe.com/reaction/538919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
SolventDichloromethaneHCID 6344—
Product(S)-4-Methoxymethyl-oxazolidin-2-oneHCID 8669435338%

Reaction Steps

TsOH (800 mg, 4.21 mmol) was added to a yellow solution of product from step 5.3 (1.013 g, 4.13 mmol) in MeOH (10 ml). The mixture was stirred at RT for 90 min. Then TsOH (140 mg, 0.74 mmol) was added and it was stirred for 70 min at RT. Then solvent was removed and the residue was dissolved in DCM (6 mL) with Triethylamine (1.44 ml, 10.32 mmol). A solution of triphosgene (0.613 g, 2.07 mmol) in DCM (4 mL) was slowly added to the mixture. The reaction mixture was stirred at RT for 2 h 30. The reaction was quenched with a few drops of water. It was then acidified to pH=4 with buffer was added and then the layers were separated. The aqueous one was extracted once more with some DCM. Organic layers were combined, dried over sodium sulfate and evaporated. The residue was purified by flash chromatography (DCM/MeOH: 100%→90% DCM) to give the title compound (231 mg, 38%). ESI-MS: 132.1 [M+H]+ (LC-MS 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865894B2
Source datasetuspto-grants-2014_10
ORD IDord-6a91e23fe26a4cbbb5df82e055bf1b5d
Source noteuspto-grants-2014_10