돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346217생성일: 2026년 10월 26일

Hydrochloric Acid → Retinoyl beta-glucuronide

https://huagongshe.com/reaction/346217

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Glucuronic AcidHCID 65041—
반응물Sodium BicarbonateHCID 516892—
반응물(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenoyl fluorideHCID 5378594—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물Retinoyl beta-glucuronideHCID 528187761.1%

반응 단계

Retinoyl fluoride (2.4 g, 7.9 mmol) was dissolved in 200 ml of acetone. D-glucuronic acid (6 g, 31 mmol) dissolved in 50 ml of water and sodium bicarbonate (970 mg) dissolved in 50 ml of water were added to the retinoyl fluoride solution. The mixture was stirred at room temperature for 20-24 hrs. The solution was neutralized with 1N HCl, diluted with water, and the product was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and then evaporated to dryness in a rotary evaporator. The residue was dissolved in 2-3 ml of diethyl ether and transferred to a silica gel (for dry column chromatography, wet packed with hexane) column. The column was developed with hexane containing diethyl ether (5-50%) to remove retinoic acid and other products. The major yellow band containing retinoyl glucuronide was next eluted with a mixture of CH2Cl2 /CH3OH (1:1). The solvent was evaporated to dryness to give solid retinoyl β-glucuronide (2.3 g, 60%). This preparation consisted mainly of the all-trans isomer, and can be used as such.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05061723
출처 데이터셋uspto-grants-1991_10
ORD IDord-f6f720e4f99c4eca8d42709384fb9f64
출처 메모uspto-grants-1991_10