HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290432Generated: October 31, 2026
Acetone → [[8-Acetyl-7-[5-(4-acetyl-3-hydroxy-2-propylphenoxy)-pentyloxy]-2-naphthalenyl]oxy]acetic acid methyl ester
https://huagongshe.com/reaction/2290432
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[2,4-Dihydroxy-3-propylphenoxy]ethanone | HCID 20232737 | — |
| Reactant | HCID 54389898 | HCID 54389898 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [[8-Acetyl-7-[5-(4-acetyl-3-hydroxy-2-propylphenoxy)-pentyloxy]-2-naphthalenyl]oxy]acetic acid methyl ester | HCID 13505605 | — |
Reaction Steps
A mixture of 1.66 g of [[8-Acetyl-7-(5-bromopentyloxy)-2-naphthalenyl]oxy]acetic acid methyl ester, 0.76 g of 1-[2,4-dihydroxy-3-propylphenoxy]ethanone and 0.81 g of anhydrous potassium carbonate in 30 ml of anhydrous acetone and 10 ml of anhydrous dimethylformamide was stirred at reflux. An additional 0.8 g of anhydrous potassium carbonate was added after 15 hours. Reflux was continued for a total of 22 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo to an oil which was treated with ether and water. The organic phase was separated and washed with 1N sodium hydroxide, water and sodium chloride solution. The black oil from concentration of the organic phase was purified by flash column chromatography to yield 1.45 g. mp 87°-89° (69%) of [[8-Acetyl-7 -[5-(4-acetyl-3-hydroxy-2-propylphenoxy)-pentyloxy]-2-napththalenyl]oxy]acetic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04616091 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-ec3cbda738574f6ea8c5963b93c0509a |
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| Source note | uspto-grants-1986_10 |
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