HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651268Generated: November 2, 2026
Sulfuric Acid → 6-Methoxy-3-pentyl-2-benzofurancarboxylic acid ethyl ester
https://huagongshe.com/reaction/1651268
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Oxo-2-(3-methoxyphenoxy)octanoic acid ethyl ester | HCID 14742771 | — |
| Product | 6-Methoxy-3-pentyl-2-benzofurancarboxylic acid ethyl ester | HCID 14742772 | 53.6% |
Reaction Steps
A mixture of 2-chloro-3-oxooctanoic acid (51.5 g) and sodium 3-methoxyphenolate (35 g) was refluxed with stirring in benzene (250 mL) for 7 hours, then stirred at room temperature overnight. The cooled reaction was washed with water (2×250 mL) and the dried (MgSO4) organic layer was evaporated to give 70 g of a brown oil. The crude product was purified by HPLC (diethyl ether-hexane; 1:19) to give 30.45 g of 3-oxo-2-(3-methoxyphenoxy)octanoic acid ethyl ester as a colorless oil. 3-Oxo-2-(3-methoxyphenoxy)octanoic acid ethyl ester (21.5 g) was added over 1 hour with stirring to sulfuric acid (22 mL) at -10° C. After 1 hour at -10° C., the reaction was diluted carefully with ice (400 g) and then extracted with diethyl ether (2×400 mL). The organic extracts were washed in turn with saturated sodium bicarbonate solution and with brine, then were combined, dried (MgSO4) and evaporated. The crude reaction product was crystallized from hexane to give 10.86 g of 6-methoxy-3-pentyl-2-benzofuranecarboxylic acid ethyl ester, mp 38°-41° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04927838 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-4e62deefc2224fe582df727f9df3c0f0 |
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| Source note | uspto-grants-1990_05 |
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