HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917533Generated: October 31, 2026
Dimethylformamide → HCID 58963161, compound
https://huagongshe.com/reaction/917533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 5-Bromo-7-ethyl-3-methyl-1-benzofuran | HCID 58963156 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58963161 | HCID 58963161 | 41.9% |
Reaction Steps
5-Bromo-7-ethyl-3-methylbenzofuran 31 (21.25 g, 89 mmoles) was dissolved in dry THF (470 ml) and cooled to −78° C. under a nitrogen atmosphere. Sec-butyl lithium (69.8 ml of a 1.4 M solution, 98 mmoles) was added drop wise to the cooled reaction. The reaction mixture turned a reddish color. Dimethylformamide (51.6 ml, 666 mmoles) was added to the reaction at −78° C. The reaction was allowed to warm to room temperature and stirred overnight. The reaction was poured into 800 ml of ice/ethyl acetate and the organic layer separated. The aqueous layer was washed with ethyl acetate and the combined organic layer washed with water. The solution was dried over sodium sulfate, filtered, and the solvent removed in vacuo. The crude product was purified by flash chromatography (750 g silica, 8% ethyl acetate in hexanes) to yield 7.02 g of 7-ethyl-3-methylbenzofuran-5-carbaldehyde 32.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273886B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-2b62800637a6488da2c6c49ba76fdfa5 |
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| Source note | uspto-grants-2007_09 |
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