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Diethyl Ether → N-amino-2-(1-butynyl)-4-methoxypyridinium mesitylenesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine | HCID 11830845 | — |
| 反応物 | 2-(1-Butynyl)-4-methoxypyridine | HCID 21984661 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-amino-2-(1-butynyl)-4-methoxypyridinium mesitylenesulfonate | HCID 21984631 | — |
反応手順
To a solution of the obtained 2-(1-butynyl)-4-methoxypyridine (10.0 g) in dichloromethane (100 mL) there was added dropwise a solution of O-mesitylenesulfonylhydroxyamine (16.0 g) in dichloromethane (100 mL) at 0° C., and the mixture was stirred for 1 hour. Diethyl ether (250 mL) was added to the reaction mixture, and the precipitated solid was suction filtered and dried to obtain N-amino-2-(1-butynyl)-4-methoxypyridinium mesitylenesulfonate as a white salt (20.7 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07091215B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-0fbfc8c11b524a2cb943421f7379b2a2 |
| 出典メモ | uspto-grants-2006_08 |