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HRID 493030생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/493030

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물TrimethylsilylacetyleneHCID 66111—
반응물1-Bromo-4-propylbenzeneHCID 136374—
촉매TriphenylphosphineHCID 11776—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매WaterHCID 962—
생성물1-(4-n-Propylphenyl)-2-trimethylsilylacetyleneHCID 1935340187.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534547B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-41c7fd2116914f8b8f5c9d25ee7d1452
출처 메모uspto-grants-2009_05