ChemicalBook--->CAS DataBase List--->5747-92-2

5747-92-2

5747-92-2 Structure

5747-92-2 Structure
IdentificationMore
[Name]

Ethyl 1-benzylpyrrolidine-3-carboxylate
[CAS]

5747-92-2
[Synonyms]

1-BENZYL-PYRROLIDINE-3-CARBOXYLIC ACID ETHYL ESTER
ETHYL 1-BENZYL-PYRROLIDINE-3-CARBOXYLATE
ETHYL 1-BENZYL-PYRROLIDINE-3-CALATE
[Molecular Formula]

C14H19NO2
[MDL Number]

MFCD04039852
[Molecular Weight]

233.31
[MOL File]

5747-92-2.mol
Chemical PropertiesBack Directory
[Boiling point ]

118-120 °C(Press: 0.75 Torr)
[density ]

1.099±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Liquid
[pka]

8.43±0.40(Predicted)
[color ]

Pale yellow
[InChI]

InChI=1S/C14H19NO2/c1-2-17-14(16)13-8-9-15(11-13)10-12-6-4-3-5-7-12/h3-7,13H,2,8-11H2,1H3
[InChIKey]

CYPXEPWPTXKUPL-UHFFFAOYSA-N
[SMILES]

N1(CC2=CC=CC=C2)CCC(C(OCC)=O)C1
[CAS DataBase Reference]

5747-92-2(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P301+P310
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Uses]

Ethyl 1-benzylpyrrolidine-3-carboxylate
[Synthesis]

Ethanol

64-17-5

1-BENZYL-PYRROLIDINE-3-CARBONITRILE

10603-52-8

Ethyl 1-benzylpyrrolidine-3-carboxylate

5747-92-2

General procedure for the synthesis of ethyl 1-benzylpyrrolidine-3-carboxylate from ethanol and 1-benzylpyrrolidine-3-carbonitrile: A solution of 1-benzylpyrrolidine-3-carbonitrile (1.5 g, 7.9 mmol) in ethanol (40 mL) was treated with a dioxane solution (20 mL) in 4 M HCl and stirred overnight at room temperature. Upon completion of the reaction, the reaction mixture was cooled to 0 °C and the pH was adjusted to neutral with saturated aqueous NaHCO3 solution, followed by extraction with ethyl acetate (EtOAc). The organic layers were combined, dried with anhydrous Na2SO4 and concentrated under reduced pressure. Purification by fast column chromatography (eluent: 35-50% EtOAc/hexane) afforded ethyl 1-benzylpyrrolidine-3-carboxylate (1.1 g, 58% yield).

[References]

[1] Patent: WO2003/103669, 2003, A1. Location in patent: Page 71-72
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 1-benzylpyrrolidine-3-carboxylate(5747-92-2)1HNMR
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