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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133673생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/133673

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Indole-3-pyruvic acidHCID 803—
반응물Pyruvic AcidHCID 1060—
반응물Sodium HydroxideHCID 14798—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물4-Hydroxy-4-(3-indolylmethyl)-2-ketoglutaric acidHCID 10149460—
용매Sodium CarbonateHCID 10340—
생성물2-Hydroxy-4-(hydroxyimino)-2-[(1H-indol-3-yl)methyl]pentanedioic acidHCID 58906082—

반응 단계

After 1.0 g (4.92 mmol) of indole-3-pyruvic acid was added to and dissolved in 10 ml of aqueous saturated sodium carbonate solution, the resulting solution was adjusted to pH 12.55 using aqueous 25% sodium hydroxide solution. After 1.3 g (14.8 mmol) of pyruvic acid was added, the resulting solution was adjusted to pH 12.6 using aqueous 25% sodium hydroxide solution, for reaction at ambient temperature for 2 hours, to obtain a reaction solution containing 4-hydroxy-4-(3-indolylmethyl)-2-ketoglutaric acid. 1.37 g (19.7 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 stirred 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 0.52 g of 4-hydroxy-4-(3-indolylmethyl)-2-hydroxyiminoglutaric acid (1.5 mmol; a yield, 31% vs. indole-3-pyruvic acid) in crystal form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390909B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-5b1f893879d748b084ee61b6e20dec91
출처 메모uspto-grants-2008_06