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N-bromobutanimide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylpheny)-5-bromothiazoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine | HCID 54225833 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-Ethoxycarbonylimino-3-(3-trifluoromethylpheny)-5-bromothiazoline | HCID 54096993 | 45.3% |
反応手順
A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine (1.6 g) and N-bromosuccinimide (2 g) in chloroform (50 ml) was refluxed for 10 hours. After cooling, the reaction mixture was washed with an aqueous sodium sulfite solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.9 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromothiazoline (Compound No. 30).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05244863 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-be24221918f44d34a8f5c8d9a0afeeda |
| 出典メモ | uspto-grants-1993_09 |