HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899385Generated: October 30, 2026
Benzyl chloroformate → Benzyl 3-pyrroline-1-carboxylate
https://huagongshe.com/reaction/1899385
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Pyrroline | HCID 66059 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 3-pyrroline-1-carboxylate | HCID 643471 | 78.5% |
Reaction Steps
To a solution of 3-pyrroline (1.3 g, 18.8 mmol) and anhyd. potassium carbonate (15.3 g, 144.6 mmol) in methylene chloride (30 mL) was added dropwise benzyl chloroformate (7.4 g, 43.4 mmol) at 0° C. and stirred for 20 min. The reaction mixture was warmed to room temperature and stirred further for 2 hrs. The mixture was washed with cold water (30 mL) and brine (20 mL) and dried (MgSO4). After evaporation of solvents, the residue was purified by flash column chromatography (EtOAc/hexane (1:10)) to give 1-benzyloxycarbonyl-3-pyrroline (3 g, 78%). To a solution of catalytic amount of osmium tetroxide in water (15 mL) and acetone (7 ml) was added N-methylmorpholine 1H2O (479 mg, 3.5 mmol) and 1-benzyloxycarbonyl-3-pyrroline (600 mg, 3.0 mmol), and stirred overnight. To the reaction mixture were added sodium hydrosulfite (0.1 g) and florisil (2 g) and stirred for 30 min. The reaction mixture was filtered and washed with acetone (10 mL×2). The combined organic solution was dried (MgSO4), evaporated, and purified by flash column chromatography (EtOAc/hexane (1:1) -EtOAc only) to give meso-1-benzyloxycarbonyl-3,4-dihydroxypyrrolidine (586 mg, 84%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05571909 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-1342ed194a544a35960275845bf8ac87 |
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| Source note | uspto-grants-1996_11 |
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