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185175

Sigma-Aldrich

1-Benzyl-3-pyrrolidinone

98%

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About This Item

Empirical Formula (Hill Notation):
C11H13NO
CAS Number:
Molecular Weight:
175.23
Beilstein/REAXYS Number:
1526217
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

refractive index

n20/D 1.539 (lit.)

bp

77 °C/0.01 mmHg (lit.)

density

1.091 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

O=C1CCN(C1)Cc2ccccc2

InChI

1S/C11H13NO/c13-11-6-7-12(9-11)8-10-4-2-1-3-5-10/h1-5H,6-9H2

InChI key

DHGMDHQNUNRMIN-UHFFFAOYSA-N

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General description

The equilibrium constant for the ketoreductase-catalyzed reduction reaction of 1-benzyl-3-pyrrolidinone has been measured in n-hexane. 1-Benzyl-3-pyrrolidinone on enzymatic asymmetric reduction yields enantiopure 1-benzyl-3-hydroxypyrrolidine, well known intermediate for various drugs.

Application

1-Benzyl-3-pyrrolidinone was used as starting reagent in the synthesis of vinyl triflate. It was used to prepare chiral, alkenyl sulfoximines leading to highly functionalized diazabicycles.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

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Facile synthesis of 3-arylpyrroles by tandem Suzuki-dehydrogenation reaction.
Lee C-W and Chung YJ.
Tetrahedron Letters, 41(18), 3423-3425 (2000)
Synthesis, 2224-2224 (2006)
Practical synthetic process for enantiopure 1-benzyl-3-hydroxypyrrolidine.
Morimoto M and Sakai K.
Tetrahedron Asymmetry, 19(12), 1465-1469 (2008)
A thermodynamic study of ketoreductase-catalyzed reactions 5. Reduction of substituted ketones in n-hexane.
Tewari YB, et al.
The Journal of Chemical Thermodynamics, 40(4), 661-670 (2008)

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