HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647049Generated: October 29, 2026
Hydrochloric Acid → HCID 12906154, compound
https://huagongshe.com/reaction/647049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | HCID 12824089 | HCID 12824089 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12906154 | HCID 12906154 | — |
Reaction Steps
To a solution of 2,3-dimethoxy-5-methyl-6-(8'-ethoxycarbonyloctyl)-1,4-benzoquinone (formula I-2 wherein R=H3CO, n=7, in the form of ethylester) (0.8 part) in diethyl ether (10 volume parts), followed by the addition of a 30% solution (20 volume parts) of potassium hydroxide containing sodium hydrosulfite. The mixture was refluxed for 1 hour. After cooling, the reaction mixture was rendered acidic with hydrochloric acid and extracted with diethyl ether. The ethereal extract was washed with water and shaken together with a solution of ferric chloride. The ethereal layer was washed with water and dried over anhydrous sodium sulfate. The diethyl ether was distilled off under reduced pressure and the resulting residue was crystallized from diethyl ether-hexane. The procedure provided 2,3-dimethoxy-5-methyl-6-(8'-carboxyoctyl)-1,4-benzoquinone (formula I-2 wherein R=H3CO, n=7, in the free form) (0.53 part) as orange-colored needles melting at 39°-40.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04407757 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-f793d34cb2774e2c937b2da5bea0e0e4 |
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| Source note | uspto-grants-1983_10 |
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