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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235540Generated: October 30, 2026

Methyl morpholine oxide → HCID 86750262, compound

https://huagongshe.com/reaction/235540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 86750263HCID 86750263—
ReactantHCID 178418268HCID 178418268—
CatalystOsmium TetroxideHCID 30318—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86750262HCID 86750262—

Reaction Steps

Combine (S)-N-(3,4-dichlorobenzyl)-N-methyl-2-[N'-(t-butoxycarbonyl)-allylamino]-3-(naphth-2-yl)-propionamide (0.26 g, 0.50 mmol), N-methylmorpholine-N-oxide (0.065 g, 0.55 mmol), acetone (10 mL), tetrahydrofuran (5 mL), and water (5 mL). Add osmium tetraoxide (0.26 mL, 0.04M in THF, 0.042 mmol) and stir under an inert atmosphere for 18 hours. Pour the reaction mixture into a saturated solution of sodium bisulfite and extract the intermediate diol into ethyl acetate. Dry the separated organic layer over MgSO4, filter, and evaporate in vacuo to give the crude diol which is used without further purification. Dissolve the crude diol in chloroform (10 mL). Add a solution of lead tetraacetate (0.24 g, 0.55 mmol) in chloroform (10 mL). Stir for 30 minutes and then pour the reaction mixture into a saturated solution of sodium bicarbonate. Extract with dichloromethane and separate the organic layer. Dry the separated organic layer over MgSO4, filter and evaporate in vacuo to give the title compound which may be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597845
Source datasetuspto-grants-1997_01
ORD IDord-b5deefc2c61e417eb5be53c23c0423c3
Source noteuspto-grants-1997_01