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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359363Generated: October 27, 2026

Water → 2-Benzyl-6-(cis-3,4-dihydroxypyrrolidine-1-yl)pyridine

https://huagongshe.com/reaction/1359363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ThiosulfateHCID 24477—
ReactantMethyl morpholine oxideHCID 82029—
Reactant2-Benzyl-6-(3-pyrroline-1-yl)pyridineHCID 18182236—
Reactant2-Benzyl-6-(pyrrolidine-1-yl)pyridineHCID 18182452—
CatalystOsmium TetroxideHCID 30318—
SolventAcetoneHCID 180—
Solventtert-ButanolHCID 6386—
Product2-Benzyl-6-(cis-3,4-dihydroxypyrrolidine-1-yl)pyridineHCID 69758731—

Reaction Steps

2.3 ml of a 2-methyl-2-propanol solution containing 2.5% osmium tetraoxide was added dropwise little by little into a mixture of 11.8 g of a mixture of 2-benzyl-6-(3-pyrroline-1-yl)pyridine and 2-benzyl-6-(pyrrolidine-1-yl)pyridine, 23.5 g of aqueous 50% N-methylmorpholine-N-oxide solution, 50 ml of acetone and 10 ml of water in an ice bath. After stirring for 2 hours in an ice bath, it was further stirred at room temperature overnight. A aqueous sodium thiosulfate solution was added to the reaction solution, followed by stirring at room temperature for 30 minutes. Then, the mixture was extracted with ethyl acetate, and the organic phase was washed with water and brine, and the solvent was removed. Then, the residue was subjected to silica gel column chromatography and eluted with hexane/ethyl acetate (5:1) and then with ethyl acetate, to give 4.2 g of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599917B1
Source datasetuspto-grants-2003_07
ORD IDord-a30c8827e3c549c9997591e24a74bbcf
Source noteuspto-grants-2003_07