HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Benzyl 3,4-dihydroxypyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Benzyl 3-pyrroline-1-carboxylate | HCID 643471 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Product | Benzyl 3,4-dihydroxypyrrolidine-1-carboxylate | HCID 14771964 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181277B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-d494025b343d4d24af84fb2c3a7cbd17 |
| Source note | uspto-grants-2015_11 |