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Pyridine → (3-Ethyloxetan-3-yl)methyl 3-pyridinecarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 3-(Chloromethyl)pyridine hydrochloride | HCID 23394 | — |
| 反応物 | Oxt-101 | HCID 76444 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (3-Ethyloxetan-3-yl)methyl 3-pyridinecarboxylate | HCID 19992002 | — |
反応手順
Nicotinyl chloride hydrochloride (8.9 gm.) was added to a stirred solution of 3-ethyl-3-hydroxymethyloxetane (5.8 gm.) and dry pyridine (20 ml.) in dry dichloromethane (150 ml.) at 0°. The mixture was stirred at room temperature for 4 days and poured into aqueous sodium carbonate solution. The aqueous mixture was extracted with dichloromethane. The extracts were washed with water and dried over anhydrous magnesium sulphate. The solvent was removed in vacuo. The residue was purified by chromatography on silica eluting with 5% triethylamine in dichloromethane. (3-Ethyloxetan-3-yl)methyl 3-pyridinecarboxylate was obtained as a pale yellow oil (7.0 gm.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05057504 |
| 出典データセット | uspto-grants-1991_10 |
| ORD ID | ord-e348c7bc47ba44ad998de5232bb87078 |
| 出典メモ | uspto-grants-1991_10 |