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HRID 69111作成日:2026年10月24日

Hydrochloric Acid → Tert-butyl 2-(4-bromo-2-nitrobenzoyl)-3-oxobutanoate

https://huagongshe.com/ja/reaction/69111

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Tert-butyl acetoacetateHCID 15538—
反応物Magnesium ChlorideHCID 5360315—
反応物4-Bromo-2-nitrobenzoyl chlorideHCID 18919880—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 2-(4-bromo-2-nitrobenzoyl)-3-oxobutanoateHCID 8669431564%

反応条件

温度-8 °C

反応手順

Under a nitrogen atmosphere, to a suspension of 2.28 g of magnesium chloride in 50 mL of tetrahydrofuran was added 3.80 g of tert-butyl 3-oxobutanoate at room temperature. The mixture was cooled to −8° C., and 3.9 mL of pyridine was added thereto, followed by stirring at the same temperature for 30 minutes, warming to room temperature, and further stirring for 30 minutes. The mixture was cooled to −8° C., and a solution of 5.3 g of 4-bromo-2-nitrobenzoyl chloride in 20 mL of tetrahydrofuran was added thereto, followed by stirring at the same temperature for 1 hour, warming to room temperature, and further stirring for 1.5 hours. The mixture was poured into a mixture of water and ethyl acetate, and adjusted to pH 3 with concentrated hydrochloric acid. The aqueous layer was separated, and then the organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain 4.95 g of tert-butyl 2-(4-bromo-2-nitrobenzoyl)-3 -oxobutanoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822448B2
出典データセットuspto-grants-2014_09
ORD IDord-2785f0f145504683ba851c929693a5f8
出典メモuspto-grants-2014_09