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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3-Oxo-2-(3-methoxyphenoxy)octanoic acid ethyl esterHCID 14742771—
Product6-Methoxy-3-pentyl-2-benzofurancarboxylic acid ethyl esterHCID 1474277253.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927838
Source datasetuspto-grants-1990_05
ORD IDord-4e62deefc2224fe582df727f9df3c0f0
Source noteuspto-grants-1990_05