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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215433Generated: October 30, 2026

N-Methylmorpholine N-oxide monohydrate → HCID 21948859, compound

https://huagongshe.com/reaction/2215433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methylmorpholine N-oxide monohydrateHCID 2724197—
ReactantHCID 21948811HCID 21948811—
CatalystOsmium TetroxideHCID 30318—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 21948859HCID 21948859—

Reaction Steps

336 mg (2.5 mmol) of N-methylmorpholine-N-oxide hydrate and 10.22 ml of osmium tetroxide solution in isopropanol are added at 0° C. to a solution that consists of 3.18 g (15.88 mmol) of 5-nitro-2-vinylquinoline in 140 ml of acetone and 21 ml of water, and the reaction mixture is stirred for 24 hours at room temperature. Then, the solvent is removed in a vacuum, and the residue is taken up in ethyl acetate. The organic phase is washed with water and saturated sodium chloride solution. The aqueous phase is extracted repeatedly with dichloromethane, diethyl ether and ethyl acetate. The combined organic phases are dried on sodium sulfate. After removal of the solvent and purification of silica gel with hexane-ethyl acetate (0–100%) as well as with ethyl acetate-methanol (0–20%), 1.64 g (44% of theory) of the product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109212B2
Source datasetuspto-grants-2006_09
ORD IDord-7a5e1a900e3a456f930918cf3e006970
Source noteuspto-grants-2006_09