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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712396Generated: October 29, 2026

Acetone → Benzyl 3,4-dihydroxypyrrolidine-1-carboxylate

https://huagongshe.com/reaction/712396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl morpholine oxideHCID 82029—
ReactantBenzyl 3-pyrroline-1-carboxylateHCID 643471—
ReactantSodium BisulfiteHCID 23665763—
CatalystOsmium TetroxideHCID 30318—
ProductBenzyl 3,4-dihydroxypyrrolidine-1-carboxylateHCID 14771964100%

Reaction Steps

To a solution of N-carbobenzoxy-3-pyrroline (1.00 g, 4.92 mmol, 1.0 eq) in acetone (20 mL) was added NMO (1.0 g, 7.38 mmol, 1.5 eq) followed by OsO4 (cat. 10 mg in 1 mL iPrOH). The mixture was stirred for 3 h. To this, saturated NaHSO3 aqueous solution (5 mL) was added, and the mixture was stirred for another 0.5 h. The organic phase was separated from the mixture, and the water phase was extracted with EtOAc (20 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by a silica gel column chromatography (EtOAc) to give the compound as colorless oil (1.16 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181277B2
Source datasetuspto-grants-2015_11
ORD IDord-d494025b343d4d24af84fb2c3a7cbd17
Source noteuspto-grants-2015_11