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Toluene → 2-Chloro-6-(2-oxopropyl)-isonicotinic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Isopropenyl acetate | HCID 7916 | — |
| 反応物 | Methyl 2,6-dichloroisonicotinate | HCID 93237 | — |
| 反応物 | Methoxytri-n-butylstannane | HCID 11964040 | — |
| 触媒 | Bis(tri-o-tolylphosphine)palladium(II) Dichloride | HCID 10876480 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-Chloro-6-(2-oxopropyl)-isonicotinic acid methyl ester | HCID 86081356 | 29% |
反応手順
Add methyl 2,6-dichloroisonicotinate (3.0 g, 15.0 mmol), trans-dichlorobis(tri-o-tolylphosphine)palladium (II) (196 mg, 0.25 mmol), tributyltin methoxide (2.4 g, 7.5 mmol) and toluene (20 mL) in a previously nitrogen filled sealed vessel. Flush the reactants with nitrogen again. Add isopropenyl acetate (0.85 mL, 7.75 mmol) under nitrogen and heat the sealed mixture at 100° C. overnight with vigorous stirring. Cool the reaction to room temperature, dilute with diethyl ether and filter through a filtering agent. Concentrate and purify (silica gel chromatography, eluting with 0:100 to 20:80 ethyl acetate:hexanes) to give the title compound (29%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07585885B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-6cafdc01f40e4a8093bd56662c23170e |
| 出典メモ | uspto-grants-2009_09 |