Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | 4-Methoxypyridine | HCID 69278 | — |
| Reactant | HCID 178478979 | HCID 178478979 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69012019 | HCID 69012019 | 65% |
Reaction Steps
To a solution of 4-methoxypyridine (45.871 mmol, 1.0 eq.) in dry tetrahydro-furan (200 ml) was added acetyl chloride (45.871 mmol, 1.0 eq.), followed by TMSOTf (45.871 mmol, 1.0 eq.) at room temperature. The reaction mixture was cooled to −78° C. and stirred for 1 h. PhMgCl (3.0 eq., 2M solution in THF) was added dropwise to the reaction mixture at −78° C. and mixture was stirred at same temperature for additional 1 h. The reaction mixture was quenched with 2M HCl and warmed to room temperature. The mixture was extracted with ethyl acetate, dried over sodium sulfate and solvent was evaporated under reduced pressure to get crude product which was purified by column chromatography. Yield: 65%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268814B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-82a14cff3a18420cb0c294610ccc9ee7 |
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| Source note | uspto-grants-2012_09 |
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