HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637102Generated: October 31, 2026
(+/-) Methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-3-ethynylpropionate → HCID 53907478, compound
https://huagongshe.com/reaction/1637102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (+/-) Methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-3-ethynylpropionate | HCID 15463371 | — |
| Reactant | HCID 19349977 | HCID 19349977 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 53907478 | HCID 53907478 | 82.5% |
Reaction Steps
To a solution of the compound from Example 7 (0.15 g, 0.5 mmol) and 1-iodo-3-(5-methyl-[1,3,4]oxadiazol-2-yl)benzene (0.14 g, 0.5 mmol) in triethylamine (5 mL) under an argon atmosphere was added trace tetrakis(triphenylphosphine)palladium(0) and trace copper(I) iodide. The mixture was heated at 80° C. for 0.2 h, was cooled to room temperature and was concentrated in vacuo. Purification by flash chromatography (silica gel, 50% EtOAc/hexane) provided the titled compound as a yellow oil (0.19 g, 80%). Anal. (C27H28N2O5· 0·375 H2O) calcd: C, 69.40; H, 6.20; N, 6.00. found: C, 69.23; H, 6.13;N,5.69.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06037367 |
|---|
| Source dataset | uspto-grants-2000_03 |
|---|
| ORD ID | ord-428cdb6cae7244ab932aa3b46becba8f |
|---|
| Source note | uspto-grants-2000_03 |
|---|