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2-(Tri-n-butylstannyl)thiophene → Methyl 6-thien-2-ylnicotinate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| 反応物 | HCID 178498304 | HCID 178498304 | — |
| 触媒 | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Methyl 6-thien-2-ylnicotinate | HCID 17879034 | — |
反応手順
A solution of 2.0 g of (methyl 6-hydroxypyridine-3-carboxylate, o-triflate) and 5.23 g of 2-(tributylstannyl)thiophene in 50 ml of dry toluene is stirred under nitrogen at reflux for 16 hours in the presence of tetrakis(triphenylphosphine)palladium(O). The reaction mixture is diluted with 50 ml of chloroform and filtered through a pad of diatomaceous earth. The filtrate is evaporated in vacuo to a residue which is extracted and decanted (2×100 ml) with 1:1 ether:petroleum ether. The combined extracts are evaporated in vacuo to give 1.6 g of the desired product as a residue.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05521173 |
| 出典データセット | uspto-grants-1996_05 |
| ORD ID | ord-3023e0090bc042f38e9eb76b5d347720 |
| 出典メモ | uspto-grants-1996_05 |