HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171015Generated: November 1, 2026
Dimethylformamide → 5-(3,4-dimethoxy-2-(methoxymethoxy)phenyl)isobenzofuran-1(3H)-one
https://huagongshe.com/reaction/2171015
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Bromophthalide | HCID 603144 | — |
| Reactant | [3,4-Dimethoxy-2-(methoxymethyl)phenyl]boronic acid | HCID 67462911 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Product | 5-(3,4-dimethoxy-2-(methoxymethoxy)phenyl)isobenzofuran-1(3H)-one | HCID 67466749 | — |
Reaction Steps
To a stirring solution of 3,4-dimethoxy-2-(methoxymethyl)phenylboronic acid (Compound 301) (3.5 g, 16.58 mmol) in dimethylformamide (50 mL) under nitrogen atmosphere, were added cesium carbonate (16.17 g, 49.75 mmol), tetrakis(triphenylphosphine) palladium(0) (957 mg, 0.828 mmol) and 5-bromoisobenzofuran-1(3H)-one (8.02 g, 33.14 mmol) and the resultant reaction mixture was heated to 70° C. for 3 h. The reaction mixture was filtered off and the filtrate was extracted with ethyl acetate (3×). The combined ethyl acetate layer was washed with brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure. Purification by column chromatography (silica gel, 0-30% ethyl acetate in pet ether) afforded 5-(3,4-dimethoxy-2-(methoxymethoxy)phenyl)isobenzofuran-1(3H)-one as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051290B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-144ab6755aa14343be2d601c76d81b55 |
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| Source note | uspto-grants-2015_06 |
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