HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461417Generated: October 26, 2026
Hydrochloric Acid → Retinoyl beta-glucuronide
https://huagongshe.com/reaction/1461417
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Glucuronic Acid | HCID 65041 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenoyl fluoride | HCID 5378594 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Retinoyl beta-glucuronide | HCID 5281877 | 61.1% |
Reaction Steps
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 wa stirred at room temperature for 20-24 hrs. The solution was neutralized with lN 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05075340 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-747ceb3287814642b02f6d2c67881f56 |
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| Source note | uspto-grants-1991_12 |
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