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HRID 133674作成日:2026年10月27日

Hydrochloric Acid → 2-Hydroxy-4-(hydroxyimino)-2-[(1H-indol-3-yl)methyl]pentanedioic acid

https://huagongshe.com/reaction/133674

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Indole-3-pyruvic acidHCID 803—
反応物Sodium HydroxideHCID 14798—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物4-Hydroxy-4-(3-indolylmethyl)-2-ketoglutaric acidHCID 10149460—
反応物Sodium pyruvateHCID 23662274—
溶媒Sodium CarbonateHCID 10340—
生成物2-Hydroxy-4-(hydroxyimino)-2-[(1H-indol-3-yl)methyl]pentanedioic acidHCID 5890608232%

反応手順

After 10.0 g (49.2 mmol) of indole-3-pyruvic acid was added to and dissolved in 98 ml of aqueous saturated sodium carbonate solution, the resulting solution was adjusted to pH 12.4 using aqueous 25% sodium hydroxide solution. After 16.3 g (147.6 mmol) of sodium pyruvate was added for reaction at ambient temperature for 2 hours, a reaction solution containing 4-hydroxy-4-(3-indolylmethyl)-2-ketoglutaric acid was obtained. 13.7 g (197 mmol) of hydroxylamine hydrochloride salt was added to the reaction solution while the reaction solution was adjusted to a pH value around neutrality using aqueous 25% sodium hydroxide solution, and agitated at ambient temperature for 4 hours. Using conc. hydrochloric acid, the reaction solution was adjusted to an acidic pH value, to extract the organic matter in ethyl acetate. The organic layer was rinsed with aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate and subsequently concentrated, to obtain the residue. The residue was recrystallized in aqueous 28% ammonia and ethanol, to obtain 5.51 g of 4-hydroxy-4-(3-indolylmethyl)-2-hydroxyiminoglutaric acid (16.2 mmol; a yield of 32% vs. indole-3-pyruvic acid) in crystal form.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390909B2
出典データセットuspto-grants-2008_06
ORD IDord-31384b1bd82b4cfaa6170c4e40b47500
出典メモuspto-grants-2008_06