Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614880Generated: October 25, 2026

Methanol → 5-(4H-1,3-Benzodioxin-2-yl)-2-methoxyphenol

https://huagongshe.com/reaction/614880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,4-BenzodioxanHCID 10301—
ReactantBarium methanolateHCID 13438163—
SolventBenzeneHCID 241—
Product5-(4H-1,3-Benzodioxin-2-yl)-2-methoxyphenolHCID 592377—

Reaction Steps

A 30-g. portion of the benzodioxan compound prepared in Example 1C was dissolved in 300 ml. of warm benzene, diluted with 600 ml. of methanol containing 70 mmol. of barium methoxide, and then stored 18 hours at 5° C. After adding 10 g. of ammonium acetate, volatiles were evaporated and the residue was extracted with two 500-ml. portions of chloroform. The chloroform was washed once with 500 ml. of water, the water was reextracted with 500 ml. of chloroform, and the combined chloroform extracts were washed once with 300 ml. of water. Evaporation and crystallization from diethyl ether-n-hexane gave the neutral form of the novel sweet compound (23 g., 95%), m.p. 105°-106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04146650
Source datasetuspto-grants-1979_03
ORD IDord-91f1bbd1e9284077a666d6c9a495aaed
Source noteuspto-grants-1979_03