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HRID 1258834作成日:2026年10月27日

1-(4-Bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl ester → 6-bromospiro[benzo[b][1,4]oxazine-2,1'-cyclopropan]-3(4H)-one

https://huagongshe.com/reaction/1258834

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl esterHCID 58340784—
触媒IronHCID 23925—
溶媒Acetic AcidHCID 176—
溶媒Ethyl AcetateHCID 8857—
生成物6-bromospiro[benzo[b][1,4]oxazine-2,1'-cyclopropan]-3(4H)-oneHCID 2158135993.2%

反応条件

温度60 °C

反応手順

To a stirred solution of 1-(4-bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl ester (3.5 g, 10.6 mmol) in glacial acetic acid (40 mL) was added iron powder (5.9 g, 106.1 mmol) at room temperature and the reaction mixture was heated at 60° C. for 3 h. The mixture was cooled to room temperature, diluted with ethyl acetate, and filtered through celite bed. The filtrate was concentrated, and the resulting residue was taken in ethyl acetate and washed with water and saturated sodium bicarbonate solution, then the organic layer was dried over sodium sulfate, concentrated and the resulting residue was purified by silica gel column chromatography to furnish 6-bromospiro[4H-1,4-benzoxazine-2,1′-cyclopropane]-3-one (2.51 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08466114B2
出典データセットuspto-grants-2013_06
ORD IDord-d240245aa72140a3bb92cfd635069b9c
出典メモuspto-grants-2013_06