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HRID 25542作成日:2026年10月23日

Hydrochloric Acid → HCID 178485979、化合物

https://huagongshe.com/ja/reaction/25542

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QuinolineHCID 7047—
反応物DiphosgeneHCID 10426—
反応物Sodium hydrideHCID 24758—
反応物3,4-DifluorophenolHCID 75927—
反応物HCID 178484843HCID 178484843—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178485979HCID 178485979238.5%

反応条件

温度0 °C

反応手順

4.01 g (31 mmol) of trans-4-methylamino-cyclohexanol (twice suspended in toluene and evaporated under reduced pressure to remove water) were suspended in 60 ml hexamethyldisilazane and refluxed for 2.5 h. The solution was evaporated under reduced pressure, dissolved in 80 ml CH2Cl2 and added to a cooled solution (0° C.) of 2.06 ml (17.05 mmol) trichloromethylchloroformate (diphosgene) and 4.40 ml (34.10 mmol) quinoline. The reaction was stirred for 3 h at 0° C. and evaporated. The residue and 8.47 g (65.1 mmol) 3,4-difluorophenol were dissolved in 220 ml THF, treated at 0° C. in small portions with 3.25 g (74.4 mmol) of NaH (ca 55% in oil) and 0.26 g (1.6 mmol) of KI. The reaction was stirred at room temperature over night, cooled (0° C.) and after the addition of 0.68 g (15.5 mmol) of NaH (ca 55% in oil) stirred at RT for 24 h. After the addition of 60 ml water, the pH was adjusted to pH 2 (1 N HCl) and the reaction mixture was stirred for 1 h. The reaction was partitioned between aqueous 1 N NaOH/Et2O (3×300 ml), the organic phases were dried over Na2SO4 and evaporated. The residue was dissolved in 200 ml THF/dioxane (1:1). 34 ml 1 N NaOH were added at 0° C. and the mixture was stirred for 3 h. The reaction was partitioned between water/Et2O (3×300), the organic phase was dried over Na2SO4 and evaporated to yield 11.6 g crude trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 3,4-difluoro-phenyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858651B2
出典データセットuspto-grants-2005_02
ORD IDord-67569c580ccb494c84e048ff878a96ae
出典メモuspto-grants-2005_02