HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339069Generated: October 30, 2026
Methane → (3R,4R)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylate
https://huagongshe.com/reaction/339069
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | (3R,4R)-tert-butyl 3-azido-4-methoxypyrrolidine-1-carboxylate | HCID 57349953 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3R,4R)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylate | HCID 57349954 | — |
Reaction Steps
A mixture of (3R,4R)-tert-butyl 3-azido-4-methoxypyrrolidine-1-carboxylate (2.04 g, 8.420 mmol) and PtO2 (0.096 g, 0.42 mmol) in MeOH (100 mL) was charged with hydrogen (1 atmosphere) and stirred at ambient temperature for 2 days. Charcoal (2 g) was added to the solution and. The catalyst was removed by filtration and washed with MeOH (20 mL). The solvent was removed and dried to give (3R,4R)-tert-butyl 3-amino-4-methoxypyrrolidine-1-carboxylate. It was dissolved in dioxane (10 mL) and water (10 mL). Na2CO3 (1.34 g, 12.63 mmol) was added, followed by Cbz-Cl (1.87 mL, 12.63 mmol) at ambient temperature. The reaction mixture was stirred at ambient temperature for 3 hours. Ethyl acetate (50 ml) was added. The organic layer was separated, washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue obtained was purified by flash chromatography on silica gel (1:1 hexane/ethyl acetate) to give (3R,4R)-tert-butyl 3-(benzyloxycarbonylamino)-4-methoxypyrrolidine-1-carboxylate (2.90 g, 98.3% yield) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08889704B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-c1e5cf8935134e92b23829ed2a641307 |
|---|
| Source note | uspto-grants-2014_11 |
|---|