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HRID 130882作成日:2026年10月26日

Methanol → 2-(4-Methoxyphenethylamino)cyclohexanol

https://huagongshe.com/reaction/130882

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium CarbonateHCID 11430—
反応物2-AminocyclohexanolHCID 23286—
反応物4-(2-Chloroethyl)phenyl methyl etherHCID 87513—
溶媒DimethylformamideHCID 6228—
生成物2-(4-Methoxyphenethylamino)cyclohexanolHCID 60714650—

反応条件

温度100 °C

反応手順

Mix (±)-2-aminocyclohexanol (1.5227 g, 13.2 mmol), K2CO3 (4.56 g, 33.0 mmol), and 1-(2-chloroethyl)-4-methoxybenzene (2.0 mL, 13.2 mmol) in DMF (30 mL). Heat at 100° C. for 24 hours. Cool down to room temperature and filtrate with MeOH wash. Concentrate and remove DMF azeotropically with xylenes. Take up the residue in CH2Cl2 and H2O (100 mL each). Separate the layers and extract the aqueous layer with CH2Cl2 (2×100 mL). Wash the organic layers with H2O and brine (100 mL each). Dry the combined organic layers over MgSO4, concentrate and purify by flash chromatography, eluting with 50:45:5 EtOAc/CH2Cl2/2.0 M NH3 in MeOH to afford 2-(4-methoxyphenethylamino)cyclohexanol. (1.38 g, 42%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381719B2
出典データセットuspto-grants-2008_06
ORD IDord-02ecfa8e9a624065a593c932350603ad
出典メモuspto-grants-2008_06