Production Method 1

35392-80-4

35392-77-9

80-58-0

Reaction Conditions

1.1 Reagents: Lithium diisopropylamide Solvents: Tetrahydrofuran ;  2 h, 20 - 25 °C

Reference

Reaction of Lithium Acylate α-Carbanions with Carbon Tetrabromide

Zorin, A. V.; et al, Russian Journal of Organic Chemistry, 2019, 55(10), 1527-1531

meso-2,3-diethylbutanedioic acid Preparation Products

• racemic-2,3-diethylbutanedioic acid (35392-77-9)
• meso-2,3-diethylbutanedioic acid (35392-80-4)
• 2-Bromobutyric acid (80-58-0)

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  JGQuintiere
• 3. An amide probe as a selective Al3+ and Fe3+ sensor inside the HeLa and a549 cell lines: Pictet–Spengler reaction for the rapid detection of tryptophan amino acid?
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• 4. Alternative donor substrates for inverting and retaining glycosyltransferases?
  Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367
• 5. An amorphous carbon nitride/NiO/CoN-based composite: a highly efficient nonprecious electrode for supercapacitors and the oxygen evolution reaction?
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• 595-37-9(Dimebutic acid)
• 597-43-3(2,2-Dimethylsuccinic acid)
• 610-09-3(cis-1,2-Cyclohexanedicarboxylic acid)
• 619-81-8(Cis-1,2-Cyclohexanedicarboxylic Acid)
• 97-61-0(2-Methyl-pentanoic Acid)
• 498-21-5(Methylsuccinic acid)
• 124-83-4((1R,3S)-Camphoric Acid)
• 619-82-9(trans-cyclohexane-1,4-dicarboxylic acid)
• 105-43-1(3-methylpentanoic acid)
• 99-66-1(Valproic acid)