戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1754134作成日:2026年10月23日

Benzyl Alcohol → Florpyrauxifen-benzyl

https://huagongshe.com/ja/reaction/1754134

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物Carbon DioxideHCID 280—
反応物Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
反応物FlorpyrauxifenHCID 67420724—
溶媒TetrahydrofuranHCID 8028—
生成物Florpyrauxifen-benzylHCID 7049545078%

反応条件

温度90 °C

反応手順

To a solution of 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinic acid (prepared by the methods described in U.S. Pat. No. 7,314,849 B2; 100 milligrams (mg), 0.29 millimoles (mmol)) in tetrahydrofuran (THF; 1 milliliter (mL)) was added carbonyl diimidazole (51 mg, 0.32 mmol). The reaction mixture was stirred at ambient temperature for 30 minutes (min) when carbon dioxide (CO2) evolution ceased. Benzyl alcohol (62 mg, 0.58 mmol) was added, and the reaction mixture was heated in a benchtop microwave at 90° C. for 20 min. The reaction mixture was purified by silica gel chromatography (applied directly to an Isco 40 gram (g) RediSep® column eluting with 0-100% diethyl ether (Et2O) in hexanes) to yield a white solid (147 mg, 78%): mp 132-133° C., 1H NMR (400 MHz, DMSO-d6) δ 7.50-7.33 (m, 6H), 7.29 (dd, J=8.5, 7.1 Hz, 1H), 7.13 (s, 2H), 5.37 (s, 2H), 3.92 (s, 3H); ESIMS m/z 439 ([M+H]+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09169217B2
出典データセットuspto-grants-2015_10
ORD IDord-6d8c455e4ea0473588dc440192bacff7
出典メモuspto-grants-2015_10