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HRID 493030作成日:2026年10月26日

Hydrochloric Acid → 1-(4-n-Propylphenyl)-2-trimethylsilylacetylene

https://huagongshe.com/reaction/493030

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TriethylamineHCID 8471—
反応物TrimethylsilylacetyleneHCID 66111—
反応物1-Bromo-4-propylbenzeneHCID 136374—
触媒TriphenylphosphineHCID 11776—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
生成物1-(4-n-Propylphenyl)-2-trimethylsilylacetyleneHCID 1935340187.1%

反応手順

To 15.0 g (75.4 mmol) of 1-n-propyl-4-bromobenzene were added 8.8 g (89.8 mmol) of trimethylsilylacetylene and 100 ml of triethylamine (NEt3), and the reaction system was purged with argon. Next were added 81 mg (0.4 mmol) of copper (I) iodide (CuI), 324 mg (1.2 mmol) of triphenylphosphine, and 162 mg of dichlorobistriphenylphosphine palladium (II) [PdCl2(PPh3)2] to the reaction system, and the mixture was subjected to reaction for 24 hours with heating and refluxing. After completion of the reaction, the reaction mixture was poured into an iced water, and the resultant mixture was acidified by adding hydrochloric acid. After the resultant water-insoluble oil was extracted with hexane, the hexane phase was washed with water. By removing hexane from the hexane phase, 14.2 g (65.7 mmol) of 1-(4-n-propylphenyl)-2-trimethylsilylacetylene was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534547B2
出典データセットuspto-grants-2009_05
ORD IDord-41c7fd2116914f8b8f5c9d25ee7d1452
出典メモuspto-grants-2009_05