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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614726Generated: October 31, 2026

Butylamine → (Z)-7,7-diethoxy-1-trimethylsilyl-3-hepten-1,5-diyne

https://huagongshe.com/reaction/1614726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-Chloro-1,1-diethoxy-4-pentene-2-yneHCID 54213967—
Reactant(Z)-5-chloro-1,1-diethoxy-4-pentene-2-yneHCID 86746680—
CatalystCopper iodideHCID 83717—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product(Z)-7,7-diethoxy-1-trimethylsilyl-3-hepten-1,5-diyneHCID 1456540754%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 5-chloro-1,1-diethoxy-4-pentene-2-yne (compound B, 3.8 g, 20 mmol) in 10 mL of benzene was added via cannula to a solution of palladium tetrakis(triphenyl-phosphine) (1.1 g, 0.95 mmol) and copper iodide (0.47 g, 2.46 mmol) in 20 mL benzene stirring at 25° C. under argon. Immediately thereafter, butylamine (4 mL, 40 mmol), followed by trimethylsilylacetylene (5 mL, 40 mmol) was added via syringe. The reaction vessel was wrapped in foil, and the reaction mixture was stirred at 25° C. for 4.25 h. The reaction mixture was poured into 100 mL water and 100 mL diethyl ether and extracted. The aqueous layer was reextracted with 2×40 mL of diethyl ether. The combined organic extracts were washed with 50 mL saturated aqueous NaCl, dried over Na2SO4, and concentrated in vacuo. Flash chromatography over SiO2 using 2%, then 4%, and then 5 % diethylether/pentane as eluent provided the title compound (2.7 g, 54%) as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198560
Source datasetuspto-grants-1993_03
ORD IDord-6ceba3c9637545e49b8b22823bf2fba5
Source noteuspto-grants-1993_03