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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900050Generated: October 27, 2026

Dimethylformamide → 3-[(1RS,2RS,4SR)-4-Bicyclo[2.2.1]-hept-2-yl-phenyl]-5-methoxymethyl-oxazolidin-2-one

https://huagongshe.com/reaction/1900050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPiperidineHCID 8082—
Reactant2-NorborneneHCID 10352—
Reactant(RS)-3-(4-iodophenyl)-5-methoxymethyl-oxazolidin-2-oneHCID 22636831—
CatalystBis(triphenylphosphine)palladium(II) diacetateHCID 10865532—
SolventFormic AcidHCID 284—
SolventEthyl AcetateHCID 8857—
Product3-[(1RS,2RS,4SR)-4-Bicyclo[2.2.1]-hept-2-yl-phenyl]-5-methoxymethyl-oxazolidin-2-oneHCID 70050637—

Reaction Steps

A solution of 56 mg of bis-(triphenylphosphine)-palladium (II) diacetate, 0.5 g of (RS)-3-(4-iodophenyl)-5-methoxymethyl-oxazolidin-2-one, 0.16 g of bicyclo[2.2.1]hept-2-ene, 0.5 ml of piperidine, 1 ml of dimethylformamide and 0.15 ml of formic acid was stirred for 3 hours under an argon atmosphere. The reaction mixture was diluted with 50 ml of ethyl acetate and the separated precipitate was removed. The filtrate was extracted twice with 20 ml of water each time, the organic phase was dried over magnesium sulfate and the solvent was distilled off. The brown oil obtained was chromatographed on a 30-fold amount of silica gel with ethyl acetate/hexane (7:3), with 0.43 g of uniform product being obtained after crystallization in ethyl acetate/hexane while cooling. The racemic (1:1) diastereomer mixture melted at 83°-84°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574055
Source datasetuspto-grants-1996_11
ORD IDord-edeac957a11f46438998f5309f817f20
Source noteuspto-grants-1996_11