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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477421생성일: 2026년 10월 23일

Nitrophenylgalactosides → (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal

https://huagongshe.com/ko/reaction/477421

반응식

참여 물질

역할이름HCID투입량
반응물NitrophenylgalactosidesHCID 96647—
반응물Sodium BicarbonateHCID 516892—
생성물(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 3037556—

반응 조건

온도37 °C

반응 단계

To a solution containing 30.12 g (100 mmol) o-nitrophenyl-β-D-galactoside in 1000 ml distilled water buffered at pH 6.8 with 0.5M phosphate buffer and maintained at 37° C. is added 10 mg of monoclonal antibodies prepared according to Example 6. The reaction mixture is gently agitated for 2.0 hours. The monoclonal antibodies are then recovered from the reaction mixture by ultrafiltration. The filtrate is then cooled to 10° C. and treated with 9.2 g (110 mmol) sodium bicarbonate. The D-galactose is recovered by extracting the filtrate with three 100 ml portions of diethyl ether. The ether portions are combined, washed once with 1.0N sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated under reduced pressure to yield D-galactose. The aqueous portion is then combined with the sodium bicarbonate wash and acidified to pH 3 by the addition of 5N hydrochloric acid. The acidified aqueous portion is then extracted three times with ether. The etheral extracts are combined, dried over magnesium sulfate, filtered and concentrated at reduced pressure to yield o-nitrophenol. The o-nitrophenol and D-galactose may be further purified by HPLC or by recrystallization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04888281
출처 데이터셋uspto-grants-1989_12
ORD IDord-ef615e3efaa140f0a2da634a16cb0614
출처 메모uspto-grants-1989_12