HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727344Generated: November 1, 2026
Water → 2-(2-Fluoro-4-pyridyl)-1-(3-methylphenyl)ethanone
https://huagongshe.com/reaction/1727344
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Fluoro-4-methylpyridine | HCID 2737403 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Fluoro-4-pyridyl)-1-(3-methylphenyl)ethanone | HCID 11543157 | 52% |
Reaction Steps
Under an argon atmosphere, a solution of diisopropylamine (44 mL, 0.31 mol) in anhydrous tetrahydrofuran (300 mL) was cooled to −78° C., and to this was added dropwise a 1.6 M n-butyllithium hexane solution (190 mL, 0.31 mol) with stirring. After completion of the addition, the solution was stirred for 10 minutes, subsequently, a solution of 2-fluoro-4-methylpyridine (34.5 g, 0.31 mol) in anhydrous tetrahydrofuran (30 mL) was added. The reaction mixture was stirred for 30 minutes at −10° C. The reaction solution was cooled to −78° C., and a solution of N-(3-methylbenzoyl)propyleneimine (52 g, 0.30 mol) in anhydrous tetrahydrofuran (30 mL) was added dropwise. After completion of the addition, the mixture was stirred for 2 hours at room temperature. To the reaction mixture was added water (100 mL), and extracted with ethyl acetate. The extracted solution was washed with water, dried, then, the solvent was distilled off. The residue was recrystallized from isopropyl ether to obtain a title compound (35 g, yield 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07495018B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-bbd2c0efbfb9483888e56ff24a6de0f5 |
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| Source note | uspto-grants-2009_02 |
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