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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 2-Benzyl-6-(3-pyrroline-1-yl)pyridine | HCID 18182236 | — |
| Reactant | 2-Benzyl-6-(pyrrolidine-1-yl)pyridine | HCID 18182452 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-Benzyl-6-(cis-3,4-dihydroxypyrrolidine-1-yl)pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599917B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-a30c8827e3c549c9997591e24a74bbcf |
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| Source note | uspto-grants-2003_07 |
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