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Hydroxyamine hydrochloride → (3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 反応物 | (3-Bromothien-2-yl) (3-methoxyphenyl)methanone | HCID 21915416 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | (3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime | HCID 72727313 | 87% |
反応手順
A mixture prepared from 7 g of (3-bromothien-2-yl) (3-methoxyphenyl)methanone, 3.09 g of hydroxyamine hydrochloride and 40 ml of pyridine was stirred at room temperature overnight and thereafter heated at 100°-115° C. for 4 hours. The mixture was then quenched with water, the organics were extracted into ether, and the ether solution was washed with 3N hydrochloric acid and water and dried over anhydrous magnesium sulfate. Evaporation of the ether left a residue which crystallized upon standing overnight. The crude solid was passed through a column (alumina packed in hexane) with 15% ether/hexane used as an eluent. The solid was recrystallized from ether/hexane to give a crystalline product (6.4 g, m.p. 100°-103° C.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04728651 |
| 出典データセット | uspto-grants-1988_03 |
| ORD ID | ord-62b2f143b8034ec8b624b7d065859d69 |
| 出典メモ | uspto-grants-1988_03 |