HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647052Generated: October 31, 2026
Hydrochloric Acid → 2,3,5-Trimethyl-6-(5'-carboxy-1'-hydroxypentyl)-1,4-benzoquinone
https://huagongshe.com/reaction/647052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium nitrosodisulfonate | HCID 3032624 | — |
| Reactant | 6-Hydroxy-6-(2'-hydroxy-3',4',6'-trimethylphenyl)hexanoic acid | HCID 12906146 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2,3,5-Trimethyl-6-(5'-carboxy-1'-hydroxypentyl)-1,4-benzoquinone | HCID 12906157 | — |
Reaction Steps
To a solution of 6-hydroxy-6-(2'-hydroxy-3',4',6'-trimethylphenyl)hexanoic acid (formula II-3 wherein R=H3C, X=H, Y=OH, n=4, in the free form) (0.158 part) in 5% sodium hydroxide solution (2 volume parts) and water (7 volume parts) was added Fremy's salt (1 part) at room temperature with stirring. After being stirred for 1 hour, the mixture was cooled to 0° C., acidified with cold dilute hydrochloric acid, and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resulting residue was subjected to column chromatography on silica gel and eluted with chloroform-methanol (20:1). The product was recrystallized from ethylacetate-hexane (1:2) to give 2,3,5-trimethyl-6-(5'-carboxy-1'-hydroxypentyl)-1,4-benzoquinone (formula I-3 wherein R=H3C, n=4, in the free form) (0.128 part) as brown needles melting at 130°-131.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04407757 |
|---|
| Source dataset | uspto-grants-1983_10 |
|---|
| ORD ID | ord-f49f5b0a582c402e80fe6291b02561d9 |
|---|
| Source note | uspto-grants-1983_10 |
|---|