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Diethyl Ether → N-amino-2-(1-butynyl)pyridinium 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)pyridine | HCID 21299391 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate | HCID 21984654 | 39.1% |
反応手順
To a solution of 2-(1-butynyl)pyridine (12.8 g) dissolved in dichloromethane (60 mL) was added a solution of O-mesitylenesulfonylhydroxylamine (Reference; Synthesis, 1997, 1) (20 g) in dichloromethane (132 mL) while cooling with ice, and the reaction mixture was stirred for 30 minutes. Diethyl ether (2 L) was added to the reaction mixture to precipitate crystals, which were filtered off and then dried under reduced pressure to afford a crude product of N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate (12.6 g) as colorless crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07176216B2 |
| 出典データセット | uspto-grants-2007_02 |
| ORD ID | ord-a70a37d229294fbbaa931445ece8feea |
| 出典メモ | uspto-grants-2007_02 |