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CAS No. : | 5965-53-7 | MDL No. : | MFCD00032382 |
Formula : | C9H14O5 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | NGRAIMFUWGFAEM-UHFFFAOYSA-N |
M.W : | 202.20 | Pubchem ID : | 80070 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P280-P305+P351+P338 | UN#: | |
Hazard Statements: | H302 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
33% | In tetrahydrofuran; at 0 - 20℃; for 24.0h;Inert atmosphere; | To a solution of 2-oxoglutarate ester (0.6 mmol) intetrahydrofuran (THF) (20.0 mL) at 0 C, under argonatmosphere was added NaBH4 (2.0 eq., 1.2 mmol). Themixture was stirred 24 h at room temperature and citricacid was added until the pH reaches 5-6. Then, silicagel (250 mg) was added to the reaction mixture and thesolvent was evaporated under reduced pressure. Theresidue was purified by silica gel column chromatography(EtOAc:hexane 1:1) to afford the respective alpha-hydroxyesters as a colorless oil.Diethyl 2-hydroxyglutarate (4a)Yield 33%; 1H NMR (CDCl3, 200 MHz) d 1.23 (t,J 7.7 Hz, 3H), 1.27 (t, J 7.7 Hz, 3H), 1.84-1.98 (m, 1H),2.06-2.22 (m, 1H), 2.41-2.49 (m, 2H), 3.10 (br s, 1H),4.05-4.27 (m, 5H); 13C NMR (CDCl3, 50 MHz) d 14.1, 29.3,29.7, 60.5, 61.8, 69.5, 173.1, 174.6; IR (film) n / cm-1 3500,2954, 1732, 1440, 1215, 1107; GC (FID) tR (R): 41.3 minand tR (S): 41.8 min; TLC (EtOAc:hexane 1:1) Rf = 0.40. |
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