HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647044Generated: October 26, 2026
Hydrochloric Acid → HCID 12906150, compound
https://huagongshe.com/reaction/647044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium nitrosodisulfonate | HCID 3032624 | — |
| Reactant | 6-(2-Hydroxy-3,4,6-trimethylphenyl)hexanoic acid | HCID 12906136 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 12906150 | HCID 12906150 | — |
Reaction Steps
Potassium nitrosodisulfonate (0.9 part) was added to a solution of 6-(2'-hydroxy-3',4',6'-trimethylphenyl)hexanoic acid (formula II-2 wherein R=H3C, X=H, Y=OH, n=4, in the free form) (0.111 part) in 1% sodium hydroxide (5 volume parts) and water (3 volume parts) and the mixture was stirred at room temperature for 30 minutes. Then, the reaction mixture was cooled to 0° C. and, following the addition of cold water (50 volume parts), it was rendered acidic with dilute hydrochloric acid, whereupon a yellow precipitate was obtained. Recrystallization of this precipitate from hexane-ethyl acetate (10:1) provided 2,3,5-trimethyl-6-(5'-carboxypentyl)-1,4-benzoquinone (formula I-2 wherein R=H3C, n=4, in the free form) (0.11 part) as yellow needles melting at 81°-82° 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-a5da59b8613645598318193bb278e6b1 |
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| Source note | uspto-grants-1983_10 |
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