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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970028Generated: October 31, 2026

Water → (S)-2-Cyclopropylaminomethyl-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1970028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyclopropylamineHCID 69828—
Reactanttert-butyl (2S)-2-formylpyrrolidine-1-carboxylateHCID 2734674—
ReactantSodium borohydrideHCID 4311764—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
Product(S)-2-Cyclopropylaminomethyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 6656921897.4%

Reaction Steps

3.78 mL (13 mmol) of titanium isopropoxide and 2 g (10 mmol) of (S)-1-tert-butoxycarbonyl-pyrrolidine-2-carbaldehyde are added to a solution of 1.7 mL (30 mmol) of cyclopropylamine in 10 mL of anhydrous methanol. The solution is stirred for 5 hours at room temperature then 378 mg (10 mmol) of sodium borohydride is added. Stirring is continued for a further 2 hours then 2 mL of water is added. The reaction mixture is filtered then the solvents are evaporated. Water is added and the compound is extracted with diethyl ether. The organic phases are dried over magnesium sulfate, filtered and evaporated to give 2.34 g (97%) of (S)—N-cyclopropyl-1-tert-butoxycarbonyl-pyrrolidin-2-ylmethyl-amine in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426437B2
Source datasetuspto-grants-2013_04
ORD IDord-b8e06d809fd24216af73071447713306
Source noteuspto-grants-2013_04