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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163989Generated: October 29, 2026

Acetic Anhydride → HCID 13066702, compound

https://huagongshe.com/reaction/1163989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13066676HCID 13066676—
SolventHydrogen iodideHCID 24841—
ProductHCID 13066702HCID 1306670273.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-[2-Methoxy-3-(o-tolyloxy)phenyl]acetic acid (34.0 g) was added to a mixture of acetic anhydride (50 ml) and 50% aqueous solution of hydrogen iodide (100 ml), and the mixture was refluxed under heating for an hour. The reaction mixture was poured into ice-water (1 l) and extracted with diethyl ether. The extract was washed with aqueous sodium hydrogen sulfite and water (twice) successively, dried over magnesium sulfate and then evaporated. The oily residue (34.0 g) was dissolved in acetic anhydride (50 ml), stirred at 100° C. for 1.5 hours and then evaporated. The crystalline residue (29.0 g) was recrystallized from methanol and diisopropyl ether successively to give colorless crystals of 7-(o-tolyloxy)-2,3-dihydrobenzofuran-2-one (22.0 g). mp 110°-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04367238
Source datasetuspto-grants-1983_01
ORD IDord-6c20e1885d084f3581ab52f59dbe6761
Source noteuspto-grants-1983_01