(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride

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(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride Basic information
Product Name:(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride
Synonyms:1-[(3R)-3-aminopyrrolidin-1-yl]ethan-1-one hydrochloride;(R)-1-Acetyl-3-aminopyrrolidine Hydrochloride;1-[(3R)-3-Aminopyrrolidin-1-yl]ethanone hydrochloride;(R)-1-(3-aminopyrrolidin-1-yl)ethan-1-one hydrochloride
CAS:1286208-55-6
MF:C6H13ClN2O
MW:164.63322
EINECS:
Product Categories:
Mol File:1286208-55-6.mol
(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride Structure
(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
Appearancewhite solid
Safety Information
MSDS Information
(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride Usage And Synthesis
Synthesis
(R)-tert-Butyl 1-acetylpyrrolidin-3-ylcarbamate

1257046-87-9

(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride

1286208-55-6

General procedure for the synthesis of R-1-acetyl-3-aminopyrrolidine hydrochloride from tert-butyl (R)-(1-acetylpyrrolidin-3-yl)carbamate: tert-butyl N-[(3R)-1-acetylpyrrolidin-3-yl]carbamate (Intermediate 14, 90 g, 0.39 mol) was slowly added to 1 L of HCl/MeOH solution at 0 °C. The reaction mixture was stirred at room temperature for 3 hours. After completion of the reaction, the mixture was concentrated and the residue was washed with ether to afford R-1-acetyl-3-aminopyrrolidine hydrochloride (55 g, 85% yield) as a white solid. The product was characterized by 1H NMR (300 MHz, MeOD): δ 2.12 (3H, m), 2.18-2.48 (2H, m), 3.56-3.79 (4H, m), 3.92-3.96 (1H, m). No mass ion peaks were observed; HPLC retention time tR = 2.78 min.

References[1] Patent: US2011/92526, 2011, A1. Location in patent: Page/Page column 21
(R)-1-(3-Aminopyrrolidin-1-yl)ethanone hydrochloride Preparation Products And Raw materials
Raw materials(R)-tert-Butyl 1-acetylpyrrolidin-3-ylcarbamate-->Methanol-->Hydrochloric acid
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