戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 9691作成日:2026年10月26日

Trifluoroacetic acid → Ethyl[4-(1,1-dimethyl-2-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}ethyl)-2-methylphenoxy]acetate

https://huagongshe.com/reaction/9691

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物TriethylsilaneHCID 12052—
反応物Ethyl[4-(1,1-dimethyl-2{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}-2-oxoethyl)-2-methylphenoxy]acetateHCID 21986375—
生成物Ethyl[4-(1,1-dimethyl-2-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}ethyl)-2-methylphenoxy]acetateHCID 21986315—

反応条件

温度50 °C

反応手順

To a reactivial containing ethyl[4-(1,1-dimethyl-2-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}-2-oxoethyl)-2-methylphenoxy]acetate (intermediate 106, 36 mg) was added trifluoroacetic acid (0.22 ml) and triethylsilane (0.11 ml). The vial was then sealed and heated at 50° C. for 18 hours. The reaction was then allowed to cool to room and concentrated in vacuo. Purification by flash column chromatography eluting cyclohexane-1% EtOAc/cyclohexane yielded the title compound as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091237B2
出典データセットuspto-grants-2006_08
ORD IDord-91be913968d14eb2aa60244378ae719c
出典メモuspto-grants-2006_08