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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 5-Chloro-1,1-diethoxy-4-pentene-2-yne | HCID 54213967 | — |
| Reactant | (Z)-5-chloro-1,1-diethoxy-4-pentene-2-yne | HCID 86746680 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (Z)-7,7-diethoxy-1-trimethylsilyl-3-hepten-1,5-diyne | HCID 14565407 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05198560 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-6ceba3c9637545e49b8b22823bf2fba5 |
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| Source note | uspto-grants-1993_03 |
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