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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129578Generated: October 30, 2026

Hydrochloric Acid → (S)-(-)-2-Aminomethyl-1-ethylpyrrolidine

https://huagongshe.com/reaction/129578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
Reactant114812-34-9HCID 10866443—
ReactantHCID 178496056HCID 178496056—
SolventWaterHCID 962—
Product(S)-(-)-2-Aminomethyl-1-ethylpyrrolidineHCID 643457131.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

Bis (2-methoxyethoxy)aluminium dihydride (203.4 g, 0.70 mol, approx. 70% solution in toluene) and toluene (80 ml, dried over molecular sieves A) were added to a three-necked round-bottomed flask. The temperature in the flask was increased to 40° C. and then (S)-1-ethyl-2-pyrrolidinecarboxamide (21.0 g, 0.147 mol, 95% purity on GC) was added spoonwise during 45 min. In order to maintain the temperature at approx. 40° C., cooling was necessary during the addition. The temperature was decreased below 10° C. 55 min after completed addition. Water (500 ml) was added during 15 min and the pH was adjusted to 1 by adding 115 ml concentrated HCl and 100 ml H2O. After extraction, the phases were separated and 200 ml CH2Cl2 were added to the water phase. The pH was subsequently adjusted to 13-14 by adding NaOH (40%, 50 ml). The organic phase was separated and the water phase was extracted with further portions of CH2Cl2 (200+100 ml). The combined organic phases were dried, filtered and concentrated under vacuo to afford 24.8 g crude title product (83%) in an optical purity of >99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468876
Source datasetuspto-grants-1995_11
ORD IDord-665d976b719544088cacceadc639a41e
Source noteuspto-grants-1995_11