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HRID 1297573作成日:2026年10月26日

Sulfuric Acid → Di-tert-amylcyclohexylphosphine

https://huagongshe.com/reaction/1297573

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物ChlorocyclohexaneHCID 10952—
反応物MagnesiumHCID 5462224—
反応物Di-tert-amylphosphinous chlorideHCID 23032008—
触媒Cuprous chlorideHCID 62652—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物Di-tert-amylcyclohexylphosphineHCID 2292548196.7%

反応手順

In a 300 ml four-necked flask thoroughly purged with nitrogen, 10.4 g (0.05 mol) of di-tert-amylphosphinous chloride, 0.10 g (0.001 mol (corresponding to 2% by mol)) of copper(I) chloride and 30 ml of tetrahydrofuran were placed. To the contents of the flask, a Grignard reagent solution previously prepared from 8.3 g (0.060 mol) of cyclohexyl chloride and 2.0 g (0.08 mol) of metallic magnesium in 50 ml of tetrahydrofuran was dropwise added over a period of 1 hour with maintaining the temperature at 25° C. to 30° C. After the dropwise addition was completed, stirring was conducted at a temperature of 35° C. to 40° C. for 6 hours. After the temperature of the reaction solution was returned to room temperature, 20 ml of toluene and 20 ml of a 5% sulfuric acid aqueous solution were added to the reaction solution to perform liquid separation. Then, the organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent and a low-boiling component were distilled off under reduced pressure to obtain 12.4 g (purity: 94.9%) of the aimed di-tert-amylcyclohexylphosphine as an oily substance. The yield was 90.2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07250535B2
出典データセットuspto-grants-2007_07
ORD IDord-b131fcae618b4d9db60a8b5908619afd
出典メモuspto-grants-2007_07