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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236509Generated: October 26, 2026

Tert-butyl 2-(4-aminophenyl)pyrrolidine-1-carboxylate → 4-(2-Ethoxymethyl-pyrrolidin-1-ylmethyl)-phenylamine

https://huagongshe.com/reaction/2236509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-(4-aminophenyl)pyrrolidine-1-carboxylateHCID 44607625—
Reactant1-(4-Bromo-benzyl)-2-ethoxymethyl-pyrrolidineHCID 68692922—
Product4-(2-Ethoxymethyl-pyrrolidin-1-ylmethyl)-phenylamineHCID 6869429847%

Reaction Steps

Using the same procedure described for the preparation of 2-(4-Amino-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester, the title compound is prepared from 1-(4-Bromo-benzyl)-2-ethoxymethyl-pyrrolidine (using the crude product obtained in the previous step) in 47% yield (two steps, based on crude residue, ˜85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-e08ff7ec9e804fe483703b357f3f5583
Source noteuspto-grants-2010_05