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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210049Generated: October 29, 2026

Acetic Acid → 4-METHOXYISOBENZOFURAN-1(3H)-ONE

https://huagongshe.com/reaction/2210049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactanto-HydroxyphthalsaureHCID 22292283—
SolventTetrahydrofuranHCID 8028—
Product4-METHOXYISOBENZOFURAN-1(3H)-ONEHCID 11116379—
Producto-MethoxyphthalsaureHCID 19598034—

Reaction Steps

Anhydrous 2-methoxyphthalic acid (640 mg), which was prepared with using anhydrous 2-hydroxyphthalic acid by the same procedure as reference example 12, was suspended in tetrahydrofuran (20 ml). Acetic acid (430 mg) and sodium borohydride (135 mg) were added to the suspension. The mixture was stirred for 30 min. at room temperature and for 2 hr. at 50° C. The reaction solution was cooled. 1N hydrochloric acid (7 ml) was added to the cooled solution. The solution was stirred for 15 min. The reaction solution was evaporated. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1→1:1) to give the title compound (314 mg) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457122
Source datasetuspto-grants-1995_10
ORD IDord-1920310458944ed6910bb40d0ed2e10a
Source noteuspto-grants-1995_10