HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118912Generated: October 28, 2026
Hydrochloric Acid → HCID 131714011, compound
https://huagongshe.com/reaction/2118912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 131714013 | HCID 131714013 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131714011 | HCID 131714011 | — |
Reaction Steps
A solution of 5.0 g (0.02 mole) chromic anhydride in 5.0 ml water is added with stirring and ice cooling to 50 ml pyridine. To this is added at 10° C. 4.04 g (0.01 mole) dl-5-acetoxy-4-(2-hydroxypropyl)-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran and the resulting mixture stirred at room temperature for three hours. The reaction mixture is poured into water, made alkaline (pH 8.5-9.0) with sodium carbonate, stirred for 20 minutes then acidified with dilute hydrochloric acid and extracted with methylene chloride. The organic layer is washed with sodium bicarbonate solution, water, brine, dried over magnesium sulfate and the solvent evaporated, the last of the solvent being removed in vacuo. The residue is purified by column chromatography on silica gel to obtain the desired ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04680404 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-0a060836e46848138e5ebf610f0b8bb9 |
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| Source note | uspto-grants-1987_07 |
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