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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822962Generated: October 30, 2026

Hydrochloric Acid → Benzo[b]thiophene, 7-fluoro-4-methoxy-

https://huagongshe.com/reaction/1822962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant476199-03-8HCID 23568964—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
ProductBenzo[b]thiophene, 7-fluoro-4-methoxy-HCID 22171140—

Reaction Conditions

Temperature190 °C

Reaction Steps

A mixture of 7-fluoro-4-methoxy-1-benzothiophene-2-carboxylic acid (61.4 g, 271 mmol) and copper powder (22.4 g, 352 mmol) in quinoline (500 mL) was heated at 190° C. for 1 h. Cooled to ambient and poured onto aqueous hydrochloric acid (2 N, 750 mL). Stirred with ethyl acetate (500 mL) for 15 minutes. Filtered through Celite, washing with ethyl acetate. The aqueous layer was extracted into ethyl acetate and the combined organic layers were washed with aqueous hydrochloric acid (2 N, 500 mL), water (500 mL), brine (500 mL), dried over MgSO4 and evaporated in vacuo. Purified by column chromatography, eluting silica gel with iso-hexane/diethyl ether 0–5% to give the product as a brown oil which crystallised to give the title compound (41.3 g, 84%); δH (300 MHz, CDCl3) 7.51 (1H, m, ArH), 7.38 (1H, d, ArH), 6.98 (1H, t, ArH), 6.65 (1H, dd, ArH) and 3.92 (3H, s, OCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037932B2
Source datasetuspto-grants-2006_05
ORD IDord-50cc5fb925d2488d8b72547a1b72d6db
Source noteuspto-grants-2006_05