HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900341Generated: October 28, 2026
Dimethylformamide → 2-Fluoro-3-(1-undecynyl)benzaldehyde
https://huagongshe.com/reaction/1900341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-(1-Undecynyl)fluorobenzene | HCID 18373021 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Fluoro-3-(1-undecynyl)benzaldehyde | HCID 18373057 | 45.2% |
Reaction Steps
To a solution of 2-(1-undecynyl)fluorobenzene (7.00 g) and tetrahydrofuran (70 ml) was added slowly n-butyllithium (1.6M, 17.8 ml) at -78° C. The reaction mixture was stirred at -78° C. for 1.5 hrs. Dimethylformamide (2.28 ml) was added slowly, and the solution was allowed to warm to room temperature over 1 hr, with stirring. Methylene chloride (300 ml) was added, and the solution was washed with 50% hydrochloric acid. The aqueous phase was extracted with methylene chloride. The extracts were combined, dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated. The residue was chromatographed on silica (250 g), eluting with hexane followed by ethyl acetate/hexane (1:4). The appropriate fractions were collected and evaporated to provide 3.53 g (45.2%) of product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574164 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-f256b66ce3ca4bc4a246cdad048788ac |
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| Source note | uspto-grants-1996_11 |
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