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Dimethyl 3-hydroxyglutarate

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Dimethyl 3-hydroxyglutarate Basic information

Product Name:
Dimethyl 3-hydroxyglutarate
Synonyms:
  • 3-hydroxyglutaric acid dimethyl ester
  • Dimethyl 3-hydroxypentanedioate
  • Pentanedioic acid, 3-hydroxy-, dimethyl ester
  • NISTC7250557
  • Glutaric acid, 3-hydroxy-, dimethyl ester
  • Nsc30047
  • Dimethyl 3-hydroxygl
  • 3-Hydroxy-pentanedioic Acid DiMethyl Ester
CAS:
7250-55-7
MF:
C7H12O5
MW:
176.17
Product Categories:
  • C6 to C7
  • Carbonyl Compounds
  • Esters
  • Building Blocks
  • C6 to C7
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Aliphatics
Mol File:
7250-55-7.mol
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Dimethyl 3-hydroxyglutarate Chemical Properties

Boiling point:
139-140 °C/8 mmHg (lit.)
Density 
1.192 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.442(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform
form 
Oil
pka
12.60±0.20(Predicted)
color 
Clear colourless to Pale Yellow
BRN 
1776666
InChI
InChI=1S/C7H12O5/c1-11-6(9)3-5(8)4-7(10)12-2/h5,8H,3-4H2,1-2H3
InChIKey
CUPGMRSSZADEIW-UHFFFAOYSA-N
SMILES
C(OC)(=O)CC(O)CC(OC)=O
CAS DataBase Reference
7250-55-7(CAS DataBase Reference)
NIST Chemistry Reference
Glutaric acid, 3-hydroxy-, dimethyl ester(7250-55-7)
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Safety Information

Safety Statements 
23-24/25
WGK Germany 
3
HS Code 
29181990

MSDS

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Dimethyl 3-hydroxyglutarate Usage And Synthesis

Chemical Properties

Off-White to Pale Yellow Oil

Uses

Dimethyl 3-hydroxyglutarate was used in the synthesis of two chiral fragments representing C1-11 and C12-25 of the polyene macrolide pimaricin.

Uses

Glutaric Acid derivative

General Description

Enantioselective hydrolysis and ammonolysis of dimethyl-3-hydroxyglutarate has been studied using immobilized lipase B isolated from Candida antarctica.

Synthesis

1830-54-2

7250-55-7

To a stirred solution of dimethyl 3-oxoglutarate (17.7 mL, 120.6 mmol) in methanol (315 mL) at 0 °C was added sodium borohydride (3.9 g, 102.5 mmol) in batches. After the reaction mixture was brought to room temperature, the reaction was continued with stirring for 24 hours. Upon completion of the reaction, the pH of the reaction mixture was adjusted to 5-6 by adding solid citric acid to quench the reaction. Subsequently, silica gel (about 1 g) was added to the reaction mixture and the solvent was removed by rotary evaporation. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, 1:1) to afford dimethyl 3-hydroxyglutarate (19.98 g, 94% yield) as a colorless oil.

References

[1] Journal of the Brazilian Chemical Society, 2011, vol. 22, # 1, p. 172 - 175
[2] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 17, p. 3650 - 3653
[3] Journal of Organic Chemistry, 1988, vol. 53, # 7, p. 1567 - 1569
[4] RSC Advances, 2016, vol. 6, # 27, p. 22737 - 22748
[5] Journal of the American Chemical Society, 2009, vol. 131, # 49, p. 17980 - 17985

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