関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Glycol monoethyl ether | HCID 8076 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | (3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime | HCID 72727313 | — |
| 触媒 | Cupric Chloride | HCID 24014 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 3-(3-Methoxyphenyl)thieno[2,3-d]isoxazole | HCID 14097241 | 68% |
反応手順
Reflux a mixture of (3-bromothiophen-2-yl)-(3-methoxyphenyl)methanone oxime (10 g, 0.032 mol), KOH (3.6 g, 0.064 mol dissolved in 10 mL water) and 2-ethoxyethanol (40 mL) under nitrogen for one hour at 105–110° C. Add copper chloride (0.16 g, 0.0016 mol) whereupon the reaction mixture becomes dark brown in color. Heat the reacton for an additional four hours. TLC shows that the reaction is complete. Add water and extract the organics into ether. Wash the ether phase with water, dry (MgSO4), filter and concentrate to yield an oil. Purify the oil by column (alumina) chromatography, and elute with 15% ether in hexane to obtain white crystals. Recrystallize the crystals from ether:hexane to yield the title compound (5 g, 68% Yield), m.p. 51–52° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07091199B1 |
|---|
| 出典データセット | uspto-grants-2006_08 |
|---|
| ORD ID | ord-4403c65bc86f4873a07629c666db5d15 |
|---|
| 出典メモ | uspto-grants-2006_08 |
|---|