Ethyl 1-benzylpiperidine-4-carboxylate

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Products Intro: Product Name:Ethyl 1-benzylpiperidine-4-carboxylate
CAS:24228-40-8
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CAS:24228-40-8
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CAS:24228-40-8
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CAS:24228-40-8
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Products Intro: Product Name:Ethyl 1-benzylpiperidine-4-carboxylate
CAS:24228-40-8
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Ethyl 1-benzylpiperidine-4-carboxylate manufacturers

Ethyl 1-benzylpiperidine-4-carboxylate Basic information
Synthesis
Product Name:Ethyl 1-benzylpiperidine-4-carboxylate
Synonyms:RARECHEM AH CK 0037;AKOS 225-01;1-BENZYLPIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER;ETHYL 1-BENZYL-4-PIPERIDINECARBOXYLATE;ETHYL 1-BENZYLPIPERIDINE-4-CARBOXYLATE;BUTTPARK 33\04-91;1-(Phenylmethyl)-4-piperidinecarboxylic Acid Ethyl Ester;1-(Phenylmethyl)piperidine-4-carboxylic Acid Ethyl Ester
CAS:24228-40-8
MF:C15H21NO2
MW:247.33
EINECS:246-094-9
Product Categories:Piperidine;Heterocyclic Compounds;Aromatics;Heterocycles
Mol File:24228-40-8.mol
Ethyl 1-benzylpiperidine-4-carboxylate Structure
Ethyl 1-benzylpiperidine-4-carboxylate Chemical Properties
Boiling point 122°C (0.5 mmHg)
density 1.037 g/mL at 25 °C
refractive index 1.5120-1.5160
Fp >110℃
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Hexanes (Slightly), Methanol (Slightly)
form clear liquid
pka7.93±0.10(Predicted)
color Colorless to Light red
CAS DataBase Reference24228-40-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-25
Safety Statements 24/25-45
RIDADR UN 2810 6.1 / PGIII
Hazard Note Irritant
HS Code 29333990
MSDS Information
Ethyl 1-benzylpiperidine-4-carboxylate Usage And Synthesis
SynthesisEthyl isonipecotate (50 g, 0.31 mol) was dissolved in toluene (150 mL) in a round bottom flask, charged with potassium carbonate (60 g, 0.43 mol) and stirred for 15 min. Benzyl chloride (42 g, 0.31 mol) was charged and the reaction mass was refluxed for 4 h at 100 °C. Upon completion of the reaction as marked by TLC (hexane:ethyl acetate; 2:1), the reaction mass was cooled to room temperature and quenched with water (100 mL), stirred and the organic phase was separated. The aqueous phase was again extracted with toluene (100 mL). Combined organic phase was washed twice with saturated brine solution (50 mL). Remove toluene in vacuo to obtain Ethyl N-benzylpiperidine-4-carboxylate ( 6.97 g, 91 %) as a yellow liquid.
Ethyl 1-benzylpiperidine-4-carboxylate
Chemical PropertiesColourless Oil
Ethyl 1-benzylpiperidine-4-carboxylate Preparation Products And Raw materials
Tag:Ethyl 1-benzylpiperidine-4-carboxylate(24228-40-8) Related Product Information
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