化工社化工社 化学情報印刷レポート · 研究参考用
m-Fluorobenzenethiol → 5-(3-Fluorophenylthio)furan-3-carboxylic Acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | m-Fluorobenzenethiol | HCID 75710 | — |
| 反応物 | 5-Bromofuran-3-carboxylic acid | HCID 13333560 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-(3-Fluorophenylthio)furan-3-carboxylic Acid | HCID 21162522 | — |
反応手順
By the procedure of Example 13, m-fluorothiophenol (3.0 g., 23.4 mmoles) was reacted with cuprous oxide (1.67 g., 11.7 mmoles) in 30 ml. of dimethylformamide and then reacted further with 5-bromofuran-3-carboxylic acid in 30 ml. of dimethylformamide. Isolation of crude solids (920 mg.) was according to Example 9. Recrystallization from methanol/water, which included decolorization with activated carbon, gave purified 5-(3-fluorophenylthio)furan-3-carboxylic acid (500 mg., m.p. 101°-103° C., m/e 238).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04282246 |
| 出典データセット | uspto-grants-1981_08 |
| ORD ID | ord-5abfd09d527643009f612c380d3e5e60 |
| 出典メモ | uspto-grants-1981_08 |