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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant(3R,4R)-tert-butyl 3-azido-4-methoxypyrrolidine-1-carboxylateHCID 57349953—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
Product(3R,4R)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-c1e5cf8935134e92b23829ed2a641307
Source noteuspto-grants-2014_11