Hydrochloric Acid → 4-Benzyl-4-hydroxy-2-ketoglutaric acid

HRID 899033

反応式

HRID 899033 の反応式
[C:1]1([CH2:7][C:8](=[O:12])[C:9]([OH:11])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:13]([CH2:18]C(O)=O)([C:15]([OH:17])=[O:16])=[O:14].[OH-].[K+].Cl>>[C:1]1([CH2:7][C:8]([OH:12])([C:9]([OH:11])=[O:10])[CH2:18][C:13](=[O:14])[C:15]([OH:17])=[O:16])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 970Oxaloacetic AcidHCID 997Phenylpyruvic acidHCID 14797Potassium Hydroxide

生成物 1

HCID 101714744-Benzyl-4-hydroxy-2-ketoglutaric acid収率 37%

実験手順

Phenyl pyruvic acid (5.0 g, 30.5 mmol) and 12.1 g (91.4 mmol) of oxaloacetic acid were added to 25 mL of aqueous solution in which 13.8 g of potassium hydroxide (purity 85%) had been dissolved, and reacted at room temperature for 72 hours. The pH value of the reaction mixture was adjusted to 2.2 using concentrated hydrochloric acid, and the reaction mixture was extracted with ethyl acetate. An organic layer was washed with saturated aqueous NaCl solution, dried on magnesium sulfate anhydrate, and then concentrated. The concentrated residue was recrystallized from ethyl acetate and toluene to yield 2.8 g (11.3 mmol) of 4-phenylmethyl-4-hydroxy-2-ketoglutaric acid as crystal.

後処理

  1. dissolutionhad been dissolved
  2. customreacted at room temperature for 72 hours
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washAn organic layer was washed with saturated aqueous NaCl solution
  5. customdried on magnesium sulfate anhydrate
  6. concentrationconcentrated
  7. customThe concentrated residue was recrystallized from ethyl acetate and toluene

出典と根拠

ORDレコード
ord-c94738518824485999d7b144da974450
出典データセット
uspto-grants-2008_04
特許番号
US07354746B1

関連ノート

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