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HRID 418913作成日:2026年10月24日

Hydrochloric Acid → 2-(4-Methoxyphenyl)cyclohexanone

https://huagongshe.com/ja/reaction/418913

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4-BromoanisoleHCID 7730—
反応物CyclohexanoneHCID 7967—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物2-(4-Methoxyphenyl)cyclohexanoneHCID 25429238.4%

反応手順

Combine 4-bromoanisole (19.6 g, 104 mmol), cyclohexanone (13.2 g, 136 mmol), sodium tert-butoxide (11.8 g, 120 mmol), palladium acetate (0.47 g, 2.1 mmol), (oxy-di-2,1-phenylene)bis-diphenylphosphine (2.28 g, 4.1 mmol) and toluene (240 mL) and heated at 90° C. under nitrogen. After 18 hours, cool to room temperature and add 1N HCl (120 mL). Extract with methylene chloride and wash the combined extracts with brine. Dry the organic layer over sodium sulfate and concentrate in vacuo. Purify by flash chromatography using silica gel and 10% ethyl acetate-hexanes to yield the titled compound (8.15 g, 38%) as a white solid. 1H NMR (CDCl3) δ 7.12 (d, 2H, J=7.5 Hz), 6.92 (d, 2H, J=7.5 Hz), 3.84 (s, 3 H), 3.59 (dd, 1H, J=8.0 and 3.5 Hz), 2.60-2.45 (m, 2H), 2.29 (m, 1H), 2.18 (m, 1H), 2.04 (m, 2H), 1.85 (m, 2H). MS m/z 205 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093302B2
出典データセットuspto-grants-2012_01
ORD IDord-3913baa3e50e4a58b0542ab5d19ebd54
出典メモuspto-grants-2012_01