ChemicalBook--->CAS DataBase List--->54322-10-0

54322-10-0

54322-10-0 Structure

54322-10-0 Structure
IdentificationBack Directory
[Name]

L-GLUTAMIC BENZYL ESTER
[CAS]

54322-10-0
[Synonyms]

L-GLUTAMIC BENZYL ESTER
1,5-Pentanedioic Acid Monobenzyl Ester
1-(Phenylmethyl) Ester Pentanedioic Acid
Pentanedioic acid, 1-(phenylmethyl) ester
[Molecular Formula]

C12H14O4
[MDL Number]

MFCD00447718
[MOL File]

54322-10-0.mol
[Molecular Weight]

222.24
Chemical PropertiesBack Directory
[Boiling point ]

153-155 °C(Press: 0.05 Torr)
[density ]

1.1645 g/cm3
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.61±0.10(Predicted)
[Appearance]

Colorless to light yellow Solid-liquid mixture
[InChI]

InChI=1S/C12H14O4/c13-11(14)7-4-8-12(15)16-9-10-5-2-1-3-6-10/h1-3,5-6H,4,7-9H2,(H,13,14)
[InChIKey]

WRSDJJXJDSEUSQ-UHFFFAOYSA-N
[SMILES]

C(OCC1=CC=CC=C1)(=O)CCCC(O)=O
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

1-(Phenylmethyl) Ester Pentanedioic Acid is a useful reagent for organic synthesis.
[Synthesis]

Glutaric anhydride

108-55-4

Benzyl alcohol

100-51-6

L-GLUTAMIC BENZYL ESTER

54322-10-0

GENERAL METHOD: To a solution of glutaric anhydride (1.0 g, 10 mmol) in DMF (4 mL) was slowly added benzyl alcohol (0.94 mL, 9.09 mmol) and N,N-diisopropylethylamine (DIEA, 1.93 mL, 11 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the solvent was removed using a rotary evaporator (Speed-vac). The residue was dissolved in ethyl acetate (50 mL) and washed sequentially with saturated sodium chloride solution (10 mL x 2). The organic phase was separated and extracted with aqueous sodium bicarbonate solution (5M, 5mL x 3). The aqueous phase extracts were combined and the pH was adjusted to 4 with aqueous citric acid (5M) and extracted with ethyl acetate (30mL × 3). All ethyl acetate extracts were combined, washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give 1,5-glutaric acid monobenzoate as a white solid (1.66 g, 89% yield).

[References]

[1] Chemical Biology and Drug Design, 2018, vol. 92, # 2, p. 1403 - 1408
[2] Synthetic Communications, 2001, vol. 31, # 9, p. 1399 - 1419
[3] Journal of the American Chemical Society, 1996, vol. 118, # 29, p. 6826 - 6840
[4] Chemical Communications, 2011, vol. 47, # 17, p. 4896 - 4898
[5] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 23, p. 7507 - 7514
Spectrum DetailBack Directory
[Spectrum Detail]

L-GLUTAMIC BENZYL ESTER(54322-10-0)1HNMR
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