HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249005Generated: October 29, 2026
HCID 12851639, compound → HCID 13753870, compound
https://huagongshe.com/reaction/1249005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12851639 | HCID 12851639 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13753870 | HCID 13753870 | 57% |
Reaction Steps
A solution of 2.00 g of 1-[2-hydroxy-4-(3-hydroxypropoxy)-3-propylphenyl]ethanone in 30 ml of acetone was added dropwise over 45 minutes to a stirred, ice cooled solution of 4.0 ml of Jones reagent in 10 ml of acetone. After 15 additional minutes, the cooling bath was removed and the reaction mixture was stirred at 23° for 15 minutes. Jones reagent (0.5 ml) was added and stirring was continued for 15 minutes. The reaction mixture was concentrated in vacuo and the residue was treated with water and extracted with ether. The ether extract was washed with three portions of 1N sodium hydroxide and the aqueous layers were combined and acidified. The product was extracted with ether and the dried (over magnesium sulfate) extract was concentrated in vacuo to a solid (1.48 g). Recrystallization from ether-hexane gave 1.21 g, mp 142°-146°, (57% yield) of 3-(4-acetyl-3-hydroxy-2-propylphenoxy)propanoic acid, the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04628115 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-73c08015314d4df09b0159daf56048ad |
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| Source note | uspto-grants-1986_12 |
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