HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936222Generated: November 2, 2026
Trimethylsilylacetylene → HCID 67484047, compound
https://huagongshe.com/reaction/1936222
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 3-Cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester | HCID 67483447 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Catalyst | Iodide Ion | HCID 30165 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67484047 | HCID 67484047 | 93.6% |
Reaction Steps
A solution of 3-cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester (716 mg, 2.0 mmol) and triethylamine (2 mL, 0.01 mmol) in N,N-dimethylformamide (2 mL) was treated with trimethylsilyl acetylene (0.71 mL, 5.0 mmol). The resulting reaction mixture was degassed with argon and then treated with cooper iodide (10 mg, 0.05 mmol) and bis(triphenylphosphine)palladium (II) chloride (15 mg, 0.02 mmol). The reaction was then heated at 70° C. for 24 h. At this time, the reaction was cooled to 25° C. and concentrated in vacuo. The residue was diluted with ethyl acetate (40 mL) and washed with a half-saturated aqueous sodium chloride solution (1×20 mL). The resulting aqueous layer was back extracted with ethyl acetate (1×40 mL). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 60/40 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-trimethylsilanylethynyl-phenyl)-propionic acid methyl ester (615 mg, 93.6%) as an orange solid: mp 72-74° C.; EI-HRMS m/e calcd for C20H28O2Si (M+) 328.1858, found 328.1852.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06388071B2 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-9a780aeec1a04ecdaf62b79da8ce0e15 |
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| Source note | uspto-grants-2002_05 |
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