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HRID 1297566作成日:2026年10月26日

Sulfuric Acid → Di-tert-amylphenylphosphine

https://huagongshe.com/reaction/1297566

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ChlorobenzeneHCID 7964—
反応物MagnesiumHCID 5462224—
反応物Di-tert-amylphosphinous chlorideHCID 23032008—
触媒Copper, bis(2,4-pentanedionato-O,O')-, (SP-4-1)-HCID 5363992—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物Di-tert-amylphenylphosphineHCID 2292545695.9%

反応手順

In a 300 ml four-necked flask thoroughly purged with nitrogen, 20 ml of tetrahydrofuran, 10.4 g (0.050 mol) of di-tert-amylphosphinous chloride and 0.13 g (0.0005 mol (corresponding to 1% by mol)) of copper(II) acetylacetonate were placed. To the contents of the flask, a Grignard reagent solution previously prepared from 6.8 g (0.060 mol) of chlorobenzene and 1.9 g (0.080 mol) of metallic magnesium in 45 ml of tetrahydrofuran was dropwise added over a period of 1 hour with maintaining the temperature at 40° C. to 45° C. After the dropwise addition was completed, stirring was conducted at the same temperature for 3 hours. After the temperature of the reaction solution was returned to room temperature, gas chromatography analysis was carried out, and as a result, di-tert-amylphosphinous chloride was present in trace amounts. Thereafter, 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 12.0 g (purity: 94.4%) of the aimed di-tert-amylphenylphosphine as a viscous oily substance. The yield was 90.5%.

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-11f85162040a4f4dbb434f16e2807057
出典メモuspto-grants-2007_07