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HRID 70733作成日:2026年10月24日

Anisole → 1-Methoxy-4-(1-phenyl-cyclohexyl)-benzene

https://huagongshe.com/ja/reaction/70733

反応式

関与物質

役割名称HCID仕込み量
反応物AnisoleHCID 7519—
反応物1-PhenylcyclohexeneHCID 13043—
反応物Ethylacetate heptaneHCID 21899848—
触媒Silver(I) trifluoromethanesulfonateHCID 76223—
溶媒DichloromethaneHCID 6344—
生成物1-Methoxy-4-(1-phenyl-cyclohexyl)-benzeneHCID 11680559—

反応手順

A mixture of AuCl3 (7.6 mg, 0.025 mmol) and AgOTf (19.3 mg, 0.075 mmol) was stirred in dichloromethane (2 mL) for 30 min. Anisole (54 mg, 0.5 mmol) and 1-Phenyl-1-cyclohexene (158 mg, 1 mmol) were then added sequentially. The resulting mixture was stirred at room temperature overnight. Evaporation of the solvent under reduced pressure gave 130 mg of crude material. Flash chromatography (heptane:ethyl acetate 95:5) afforded 90 mg of a as a colorless oil. Rf=0.33 (heptane:ethyl acetate 95:5). 1H-NMR (400 MHz, CDCl3) δ 7.27-7.25 (m, 4H), 7.19 (d, 2H, J=8.8 Hz), 7.12 (m, 1H), 6.81 (d, 2H, J=8.8 Hz), 3.77 (s, 3H), 2.30-2.20 (m, 4H), 1.62-1.44 (m, 6H). 13C-NMR (100 MHz, CDCl3) δ 157.4, 149.2, 140.9, 128.4 (two carbons), 128.4 (two carbons), 127.3 (two carbons), 125.5, 113.8 (two carbons), 55.4, 45.9, 37.5 (two carbons), 26.7, 23.2 (two carbons).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822548B2
出典データセットuspto-grants-2014_09
ORD IDord-73391136d8ff4870aa0d7c405de6649a
出典メモuspto-grants-2014_09