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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403409Generated: October 30, 2026

Methylamine → tert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2403409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant1-Boc-2-FormylpyrrolidineHCID 4227815—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Producttert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylateHCID 5334660488.8%

Reaction Steps

To a suspension of 2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (2.68 g) in methanol (30 mL) at room temperature was added a solution of methylamine (831 mg) in methanol (3 mL). The reaction mixture was stirred at room temperature for 72 h and then sodium borohydride (760 mg) and molecular sieves were added. After stirring at room temperature for 2 h, the reaction mixture was filtered and the filtrate reduced in vacuo. The residue was redissolved in dichloromethane (30 mL) and washed with saturated sodium bicarbonate solution (30 mL). The combined organics were washed with brine (30 mL), dried (MgSO4) and reduced in vacuo to give 2-methylaminomethyl-pyrrolidine-1-carboxylic acid tert-butyl ester as a pale yellow oil (2.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802670B2
Source datasetuspto-grants-2014_08
ORD IDord-49bf0b221fad4bc8a811fc6ff0269e4c
Source noteuspto-grants-2014_08