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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133674생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/133674

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Indole-3-pyruvic acidHCID 803—
반응물Sodium HydroxideHCID 14798—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물4-Hydroxy-4-(3-indolylmethyl)-2-ketoglutaric acidHCID 10149460—
반응물Sodium pyruvateHCID 23662274—
용매Sodium CarbonateHCID 10340—
생성물2-Hydroxy-4-(hydroxyimino)-2-[(1H-indol-3-yl)methyl]pentanedioic acidHCID 5890608232%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390909B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-31384b1bd82b4cfaa6170c4e40b47500
출처 메모uspto-grants-2008_06