HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → 1-(5Methylpyridin-2-yl)-2-(2,3-difluoro-4-ethoxyphenyl) acetylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 2-Bromo-5-methylpyridine | HCID 564216 | — |
| Reactant | 2-Ethynyl-5-methylpyridine | HCID 13400634 | — |
| Reactant | 1-Ethoxy-2,3-difluoro-4-iodobenzene | HCID 22008078 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-(5Methylpyridin-2-yl)-2-(2,3-difluoro-4-ethoxyphenyl) acetylene | HCID 17978010 | — |
Reaction Steps
A mixture of 0.01 mol of 5-methylpyridin-2-yl-acetylene (which can be prepared from 5-methyl-2-bromopyridine by reaction with trimethylsilyl-acetylene and Pd catalyst and subsequent splitting off of the trimethylsilyl group), 0.01 mol of 4-iodo-2,3-difluorophenetole (for the preparation, see Example 9), 30 ml of triethylamine, 0.2 mmol of Pd catalyst and 0.1 mmol of CuI is stirred at room temperature for 24 hours. The reaction mixture is diluted with petroleum ether and filtered over silica gel. Evaporation and purification give 1-(5methylpyridin-2-yl)-2-(2,3-difluoro-4-ethoxyphenyl) acetylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05068053 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-e5c2e1a1e50d4ddf8f8539b7d732b4a3 |
| Source note | uspto-grants-1991_11 |