Hydrochloric Acid → 5,6-Dimethoxy-3H-isobenzofuran-1-one

A suspension of 3,4-dimethoxybenzoic acid (10 g, 54.9 mmol) in aqueous 37% HCl (126 ml, 1522 mmol) and a 37% solution in water of formaldehyde (25 ml, 54.9 mmol) were heated to 90 to 100° C. for 6 hours. Stirring was prolonged overnight at room temperature, and then the obtained insoluble material was removed by filtration. The filtrate was quenched with water (200 ml) and extracted with ethyl acetate (200 ml×3). The combined organic layers were washed with aqueous 1N NaOH (100 ml) and then with brine (2×100 ml). The organic phase was dried over Na2SO4, filtered and evaporated to dryness. The obtained yellow solid was triturated with ethyl acetate to afford 5,6-dimethoxyisobenzofuran-1(3H)-one as a white solid (3.171 g, 16.33 mmol, 30% yield). MS/ESI+ 195.0 [MH]+.

1. customthe obtained insoluble material was removed by filtration
2. customThe filtrate was quenched with water (200 ml)
3. extractionextracted with ethyl acetate (200 ml×3)
4. washThe combined organic layers were washed with aqueous 1N NaOH (100 ml)
5. dry with materialThe organic phase was dried over Na2SO4
6. filtrationfiltered
7. customevaporated to dryness
8. customThe obtained yellow solid was triturated with ethyl acetate

ORD-Eintrag

ord-ffdae374dde9431eab5bf146c727c7e1

Quelldatensatz

uspto-grants-2015_05

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09024027B2