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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337183Generated: October 29, 2026

Methyl morpholine oxide → 2-[(1R,2S,3R)-2,3-dihydroxycyclohexyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/337183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantPropan-2-one--water (1/1)HCID 18366337—
Reactant2-[(1R)-cyclohex-2-en-1-yl]-1H-isoindole-1,3(2H)-dioneHCID 58369653—
CatalystOsmium TetroxideHCID 30318—
Product2-[(1R,2S,3R)-2,3-dihydroxycyclohexyl]-1H-isoindole-1,3(2H)-dioneHCID 5836965195%

Reaction Steps

To a suspension of 2-[(1R)-cyclohex-2-en-1-yl]-1H-isoindole-1,3(2H)-dione (18) (19.9 mmol, 4.53 g) and 4-methylmorpholine-N-oxide (60 mmol, 7.01 g) in acetone/water (4:1, 62.5 mL), osmium tetroxide (0.2 mmol, 50 mg) was added. The reaction was stirred for 4 h. The mixture was concentrated and saturated sodium sulfite (40 mL) was added. It was then promptly extracted with EtOAc three times. The combined organic layers were washed with water and brine, dried over MgSO4 and concentrated to give the crude product as a white solid (4.94 g, 95% yield). Chiral HPLC [8.53 min]. Analytical data matched published data (Donohoe, J. T.; et al., J. Org. Chem., 2002, 67, 7946-7956)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889719B2
Source datasetuspto-grants-2014_11
ORD IDord-0d962995f39542ec8daa9ecf265cd1ae
Source noteuspto-grants-2014_11