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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091228Generated: November 1, 2026

Tetrahydrofuran → 4-{[1-(5-Methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}benzoic acid

https://huagongshe.com/reaction/2091228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-{[1-(5-methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}benzoateHCID 66778946—
SolventEthanolHCID 702—
Product4-{[1-(5-Methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}benzoic acidHCID 6677880190.3%

Reaction Steps

To a mixture of methyl 4-{[1-(5-methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}benzoate (1.17 g) synthesized above, tetrahydrofuran (20 mL) and ethanol (20 mL) was added 1N aqueous sodium hydroxide solution (20.0 mL), and the mixture was stirred overnight with heating under reflux, and concentrated under reduced pressure. The residue was dissolved is in water (20 mL), and 1N hydrochloric acid (20.0 mL) was added at 0° C. The resulting precipitate was collected by filtration to give the title object compound (1.02 g, 90%) as a pale-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-8288b9024e96434ca3498d97a47e4ab9
Source noteuspto-grants-2013_05