Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate

Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate
  • CAS No.:323176-93-8
Other grades of this product :
Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate Basic information
Synthesis
Product Name:Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate
Synonyms:Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate;D,L N,O-Didesmethylvenlafaxine (Venlafaxine Impurity B);ethyl 3-(dimethylamino)-2-(4-methoxyphenyl);Venlafaxine impurity 2/Venlafaxine EP Impurity B HCl/Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate hydrochloride;Ethyl (2RS)-3-(DiMethylaMino)-2-(4-Methoxyphenyl)propanoate Hydrochloride;Venlafaxine EP Impurity B HCl;ethyl 3-(dimethylamino)-2-(4-methoxyphenyl)propanoate;α-[(DiMethylaMino)Methyl]-4-Methoxybenzeneacetic Acid Ethyl Ester
CAS:323176-93-8
MF:C14H21NO3
MW:251.32
EINECS:
Product Categories:Intermediates & Fine Chemicals;Pharmaceuticals;Aromatics;Impurities
Mol File:323176-93-8.mol
Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate Chemical Properties
Boiling point 337.9±42.0 °C(Predicted)
density 1.045±0.06 g/cm3(Predicted)
storage temp. Refrigerator
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Oil
pka8.61±0.28(Predicted)
color Pale Brown to Light Brown
Safety Information
MSDS Information
Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate Usage And Synthesis
SynthesisA mixture of ethyl p-methoxyphenylacetate (4 g, 20.62 mmol), paraformaldehyde (1.05 g, 35.0 mmol) and TBAI (0.381 g, 1.03 mmol) was heated in PhMe (16 ml) at 80-85 ºC for 3.5 hours. The reaction mixture was allowed to cool. Then, a solution of Me2NH in THF was added to the reaction mixture at 0 ºC in the presence of catalytic FeCl3 (0.160 g, 0.001 mol) and stirred for 45 minutes. After completion of the reaction, 100 ml water was added to the reaction mixture and aqueous layer was acidified with conc. HCl (pH = 2). Aqueous layer was washed with DCM (3x 50 ml) and made alkaline (pH = 8) using 5% NaOH solution, extracted with DCM (3x 50 ml), washed with water, brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Column chromatographic purification over silca gel (0.5% MeOH in CHCl3) furnished aminoester 65 as a thick colourless oil (3.08 g). When the reaction was carried out without catalyst, it took 48 hours for completetion.
UsesAn impurity of Venlafaxine (impurity B).
UsesEthyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate (Venlafaxine EP Impurity B) is an impurity of Venlafaxine (impurity B).
Ethyl α-(p-Methoxyphenyl)-β-(dimethylamino)propionate Preparation Products And Raw materials

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