HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059870Generated: November 1, 2026
Ammonium Chloride → 1-(4-Isopropyloxypyridin-2-yl)-propan-2-one
https://huagongshe.com/reaction/1059870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 4-Isopropyloxy-2-methylpyridine | HCID 18667573 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-(4-Isopropyloxypyridin-2-yl)-propan-2-one | HCID 18667608 | — |
Reaction Steps
To a stirred solution of 4-isopropyloxy-2-methylpyridine (687 mg) in tetrahydrofuran (7 ml) was added a solution of n-butyllithium in n-hexane (1.63M, 3.34 ml) dropwise at −50° C. under a nitrogen atmosphere, and the mixture was warmed to 0° C. The mixture was cooled to −50° C., and N,N-dimethylacetamide (0.549 ml) was added dropwise. Then the mixture was warmed to room temperature, poured into a saturated aqueous ammonium chloride solution and extracted with ethyl acetate (100 ml). The organic layer was washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (silica gel 50 g, 25% ethyl acetate in n-hexane) to give 1-(4-isopropyloxypyridin-2-yl)-propan-2-one (652 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521643B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-3011af2c39534fe99e088b6b1340c6ef |
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| Source note | uspto-grants-2003_02 |
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