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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493030Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/493030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
EduktTrimethylsilylacetyleneHCID 66111—
Edukt1-Bromo-4-propylbenzeneHCID 136374—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelWaterHCID 962—
Produkt1-(4-n-Propylphenyl)-2-trimethylsilylacetyleneHCID 1935340187,1%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07534547B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-41c7fd2116914f8b8f5c9d25ee7d1452
Quellennotizuspto-grants-2009_05