تفاعل #47332
ord-90743fa93f484cdf8377947ed34feb74
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةThe reaction was then warmed
- 2درجة الحرارةto reflux for 5 h
- 3أخرىAt this time, the reaction was removed from the freezer
- 4أخرىThe resulting precipitate was removed by filtration
- 5تركيزThe filtrate was concentrated in vacuo
- 6أخرىPurification by Analogix flash chromatography (40 g, 1-10% ethyl acetate/hexanes)
الإجراء التجريبي
A solution of 3-(3-chloro-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester (1.41 g, 5.45 mmol) in carbon tetrachloride (30 mL) was treated with N-bromosuccinimide (1.07 g, 6.01 mmol) and benzoyl peroxide (0.15 g). The reaction was then warmed to reflux for 5 h. At this time, the reaction was cooled to 25° C. and then placed in the freezer over the weekend. At this time, the reaction was removed from the freezer and allowed to thaw. The resulting precipitate was removed by filtration. The filtrate was concentrated in vacuo. Purification by Analogix flash chromatography (40 g, 1-10% ethyl acetate/hexanes) afforded impure 4-bromo-3-(3-chloro-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester (1.59 g, 86%) as a white solid. The material was used without further purification.