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HRID 4462作成日:2026年10月24日

Acetic Acid → 4-(4-(4-Bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-penten-1-ol

https://huagongshe.com/ja/reaction/4462

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Diethyl EtherHCID 3283—
反応物Diisobutylaluminum hydrideHCID 14487—
反応物4-(4-(4-Bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-pentenoic acid, methyl esterHCID 86741998—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物4-(4-(4-Bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-penten-1-olHCID 5437276774%

反応条件

温度-78 °C

反応手順

To a solution of 4.5 g (10.6 mmol) 4-(4-(4-bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-pentenoic acid, methyl ester in 25 ml toluene at -78° C. was added dropwise over a period of 30 min, 16.5 ml of 1.5M DIBAL-H in toluene, keeping the temperature below -60° C. The mixture was stirred for 21/2 hours at -78° C. To the mixture was added 17 ml of a 75:25:6 ether:acetic acid:water mixture, keeping the temperature below -60° C. The mixture was then allowed to warm to room temperature and the solid material was filtered off. The filtrate was washed twice with saturated NaHCO3 and once with water, dried over MgSO4 and the solvent was removed by rotary evaporation. The residue was purified by HPLC, eluting with 80:20 hexane:acetone, to give 3.1 g (74%) of the product as a pale yellow oil which was used immediately in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725683
出典データセットuspto-grants-1988_02
ORD IDord-06486a43573049c0972d0737d58446eb
出典メモuspto-grants-1988_02