HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218819Generated: October 29, 2026
1,2-Dimethoxyethane → HCID 24880045, compound
https://huagongshe.com/reaction/218819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 59138495 | HCID 59138495 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 24880045 | HCID 24880045 | 55% |
Reaction Steps
A mixture of 0.022 g (0.057 mmol) of (6-methoxy-7-nitrobenzofuran-3-yl)(3,4,5-trimethoxyphenyl)methanone, 0.1 g of ammonium formate and 0.1 g of 10% palladium on carbon in 5 ml of a mixture of 1,2-dimethoxyethane and methanol (4:1) was refluxed for 30 minutes (TLC controlled reaction). After cooling to room temperature the mixture was filtered through a pad of Celite and washed with methylene chloride. The filtrates were evaporated to dryness under reduced pressure and the residue was purified by flash column chromatography to give 0.011 g (55% yield) of pure title compound as a colorless solid; 1H NMR (CDCl3) δ 3.89 (s, 6H, OMe); 3.92 (s, 6H, OMe); 4.01 (broad s, 2H, NH2); 6.95 (d, 1H, CH aromatic, J=8.54 Hz); 7.14 (s, 2H, CH aromatic); 7.46 (d, 1H, CH aromatic, J=8.54 Hz); 8.0 (s, 1H, CH furan).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198466B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-dbcc26b0615e437c9087dc5bececd0a4 |
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| Source note | uspto-grants-2012_06 |
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