HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754228Generated: November 3, 2026
Hydrochloric Acid → HCID 178516894, compound
https://huagongshe.com/reaction/1754228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,4-Naphthalenedione, 2-chloro-3-[cis-4-(4-chlorophenyl)cyclohexyl]- | HCID 11101070 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178516894 | HCID 178516894 | — |
Reaction Steps
2-[4-(4-Chlorophenyl)cyclohexyl-3-chloro-1,4-naphthoquinone (20 gm) was added to methanol (400 ml) at 25-30° C., the contents were heated to reflux and then potassium hydroxide solution (20 gm) in water (200 ml) was slowly added for 30 minutes at reflux. The reaction mass was stirred for 6 hours at reflux, to the resulting mass added hydrochloric acid (72 ml) slowly for 15 to 20 minutes at reflux and then cooled to 25-30° C. The resulting mass was further cooled to 0° C. and then stirred for 1 hour at 0-5° C. The solid was filtered, washed with water and then dried at 50-60° C. to give 18.1 gm of atovaquone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169232B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-b52231961bc14824ac1835fdde37ef5d |
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| Source note | uspto-grants-2015_10 |
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