Basic information Safety Supplier Related

ethyl 1-benzyl-4-oxo-pyrrolidine-3-carboxylate

Basic information Safety Supplier Related

ethyl 1-benzyl-4-oxo-pyrrolidine-3-carboxylate Basic information

Product Name:
ethyl 1-benzyl-4-oxo-pyrrolidine-3-carboxylate
Synonyms:
  • Ethyl 1-benzyl-4-pyrrolidone-3-carboxylate
  • ethyl-benzyl-4-oxopyrrolidine-3-carboxylate
  • 3-Pyrrolidinecarboxylicacid, 4-oxo-1-(phenylMethyl)-, ethyl ester
  • 1-Benzyl-4-oxo-pyrrolidine-3-carboxylic acid ethyl ester
  • 4-oxo-1-(phenylmethyl)-3-Pyrrolidinecarboxylic acid ethyl ester
  • ethyl 1-benzyl-4-oxo-pyrrolidine-3-carboxylate
  • 1-(benzyl)-4-keto-pyrrolidine-3-carboxylic acid ethyl ester
  • ethyl 4-oxo-1-(phenylmethyl)pyrrolidine-3-carboxylate
CAS:
1027-35-6
MF:
C14H17NO3
MW:
247.29
Mol File:
1027-35-6.mol
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ethyl 1-benzyl-4-oxo-pyrrolidine-3-carboxylate Chemical Properties

Boiling point:
358.1±42.0 °C(Predicted)
Density 
1.184
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka
10.88±0.20(Predicted)
form 
liquid
color 
Light yellow
InChI
InChI=1S/C14H17NO3/c1-2-18-14(17)12-9-15(10-13(12)16)8-11-6-4-3-5-7-11/h3-7,12H,2,8-10H2,1H3
InChIKey
XLKXIFXOWMGWNT-UHFFFAOYSA-N
SMILES
N1(CC2=CC=CC=C2)CC(=O)C(C(OCC)=O)C1
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Safety Information

HazardClass 
IRRITANT
HS Code 
2921309990
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ethyl 1-benzyl-4-oxo-pyrrolidine-3-carboxylate Usage And Synthesis

Synthesis

795-18-6

1027-35-6

General procedure for the synthesis of ethyl 1-benzyl-4-keto-3-pyrrolidinecarboxylate from ethyl 3-(benzyl(2-ethoxy-2-oxoethyl)amino)propanoate: 1127.324 g of the crude product, compound (c), was dissolved in anhydrous 2.5 L of toluene, and 243.028 g of potassium tert-butanolate was slowly added under ice bath conditions with continuous stirring for 2 hours. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction solution was adjusted to acidic by adding 4 M hydrochloric acid in an ice bath, followed by adjusting the pH to 8 with saturated sodium bicarbonate solution.The reaction mixture was extracted with ethyl acetate, and the organic phase was dried with anhydrous sodium sulfate, filtered, and then concentrated by rotary evaporator to give 376.7 g of the pink solid compound (d) in 98% yield.

References

[1] Patent: CN102584828, 2016, B. Location in patent: Paragraph 0102-0104
[2] Patent: EP1552842, 2005, A1. Location in patent: Page/Page column 302
[3] Synthetic Communications, 1996, vol. 26, # 9, p. 1657 - 1661

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