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HRID 235239作成日:2026年10月24日

Hydrochloric Acid → (2-Acetamidophenyl) cyclohexyl methanone

https://huagongshe.com/ja/reaction/235239

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AcetanthranilHCID 68236—
反応物HCID 178419651HCID 178419651—
溶媒Diethyl EtherHCID 3283—
生成物(2-Acetamidophenyl) cyclohexyl methanoneHCID 1158681324%

反応条件

温度-10 °C

反応手順

Cyclohexylmagnesium bromide (240 ml of a 2M solution in ether, 0.48 mol) in ether (200 ml) was added dropwise to a solution of 2-methyl-4H-3,1-benzoxazin-4-one (100 g, 0.62 mol) in ether (1100ml) at -10° C. over 2 h. The mixture was stirred at this temperature for 2 h, then at ambient temperature for 30 min. After cooling to -10° C. the suspension was treated with 2M HCl (600 ml), keeping the temperature below 0° C. After stirring for 15 min the layers were separated, and the ethereal layer washed sequentially with water (500 ml), 5% sodium hydroxide solution (2×500 ml) and finally water (2×500 ml). The organic layer was separated, dried (MgSO4), evaporated in vacuo and chromatographed on silica using petrol:ethyl acetate (2:1). to give (2-acetamidophenyl) cyclohexyl methanone (28 g, 24%) as a pale yellow solid. mp 66° C. 1H NMR (CDCL3, 360 MHz)-- 1.25-1.89 (10H, m), 2.23 (3H, s), 3.33 (1H, m), 7.13 (1H, dt, J=6 and 1 Hz), 7.53 (1H, dt, J=6 and 1 Hz), 7.92 (1H, d, J=6 Hz), 8.76 (1H, d, J=6 Hz), 11.73 (1H, brs).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05597915
出典データセットuspto-grants-1997_01
ORD IDord-64a3be2e61744734a55999a534fad99c
出典メモuspto-grants-1997_01