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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133666생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/133666

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Indole-3-pyruvic acidHCID 803—
반응물Oxaloacetic AcidHCID 970—
반응물Potassium HydroxideHCID 14797—
반응물Sodium HydroxideHCID 14798—
반응물Hydroxyamine hydrochlorideHCID 443297—
용매WaterHCID 962—
생성물2-Hydroxy-4-(hydroxyimino)-2-[(1H-indol-3-yl)methyl]pentanedioic acidHCID 5890608232.1%

반응 단계

After 13.8 g of potassium hydroxide (having a purity of 85% by weight) was dissolved in 50 ml of water, 5.0 g (24.6 mmol) of indole-3-pyruvic acid and 9.8 g (73.8 mmol) of oxalacetic acid were added to the resulting solution, for reaction at ambient temperature for 72 hours (about pH 13 at the start of the reaction). To the reaction solution was added 6.8 g (98.4 mmol) of hydroxylamine hydrochloride salt. Then, the reaction solution was adjusted to pH 7.5 with aqueous 4N sodium hydroxide solution. After the reaction solution had been stirred for 24 hours at ambient temperature, the reaction solution was adjusted to pH 2.6 with 6N hydrochloric acid. After extraction using ethyl acetate, the organic layer was rinsed in aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate and concentrated to dryness. The resulting residue was dissolved in 10 ml of aqueous 14% ammonia, followed by gradual dropwise addition of 70 ml of ethanol, and stirred at ambient temperature for 3 hours. The resulting slurry was filtered. The resulting crystals was dried to obtain 2.7 g (7.9 mmol) of 4-hydroxy-4-(3-indolylmethyl)-2-hydroxyiminoglutaric acid in the form of an ammonium salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390909B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-adf6a672c47c4720b3bb22af64c24cf9
출처 메모uspto-grants-2008_06