Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300159Generated: October 31, 2026

Methyl morpholine oxide → Tert-butyl 4-(2,3-dihydroxypropyl)-4-hydroxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/2300159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantOxolane--water (1/1)HCID 21881883—
ReactantTert-butyl 4-allyl-4-hydroxypiperidine-1-carboxylateHCID 21955339—
CatalystOsmium TetroxideHCID 30318—
Solventtert-ButanolHCID 6386—
ProductTert-butyl 4-(2,3-dihydroxypropyl)-4-hydroxy-1-piperidinecarboxylateHCID 22744545—

Reaction Steps

9.83 g of tert-butyl 4-allyl-4-hydroxy-1-piperidinecarboxylate was dissolved in 60 ml tetrahydrofuran/water (9:1), a solution (2.5 wt %, 2 ml) of osmium tetraoxide in tert-butyl alcohol and 6.68 g of N-methylmorpholine-N-oxide were added thereto, and the mixture was stirred at room temperature overnight. The reaction solution was evaporated, and the resulting residue was partitioned into ethyl acetate and water, washed with brine and dried over magnesium sulfate. After filtration, the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate/methanol) to give 9.11 g of tert-butyl 4-(2,3-dihydroxypropyl)-4-hydroxy-1-piperidinecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498159B1
Source datasetuspto-grants-2002_12
ORD IDord-4eb4ea90dcb64690ae507c2e0db255d6
Source noteuspto-grants-2002_12