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HRID 230455作成日:2026年10月26日
Hydrochloric Acid → 2-(2,2,2-Trifluoro-1-hydroxy-ethyl)-6-trifluoromethyl-1H-benzimidazole-5-carbonitrile
https://huagongshe.com/reaction/230455
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 3,3,3-Trifluoro-2-hydroxypropanoic acid | HCID 244896 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 4,5-Diamino-2-(trifluoromethyl)benzonitrile | HCID 52991926 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-(2,2,2-Trifluoro-1-hydroxy-ethyl)-6-trifluoromethyl-1H-benzimidazole-5-carbonitrile | HCID 86635047 | — |
反応手順
4,5-Diamino-2-trifluoromethyl-benzonitrile (4.14 g; 20.6 mmoles) and 3,3,3-trifluoro-2-hydroxy-propionic acid (4.50 g; 31.2 mmoles) were suspended in 6N HCl (7 mL; 42 mmoles) under a nitrogen atmosphere. The reaction was stirred vigorously and heated to 108° C. for 18 hrs, then cooled to room temperature. The reaction was diluted with water (100 mL) and with ethyl acetate (100 mL), then sodium bicarbonate (5.19 g; 62.0 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×40 mL). The extracts were combined, washed with water (30 mL) and brine (30 mL), then dried over Na2SO4. The filtrate was concentrated in vacuo to yield a crude dark solid which was then purified by column chromatography (SiO2; 30% ethyl acetate/CH2Cl2) to yield the title compound as a dark brown solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07566733B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-c18a7d1784284cc087d5396fc1692a5b |
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| 出典メモ | uspto-grants-2009_07 |
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