HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533110Generated: October 28, 2026
Dimethylformamide → HCID 86686878, compound
https://huagongshe.com/reaction/533110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-(5-Bromo-2-hydroxy-phenylethynyl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 86686877 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86686878 | HCID 86686878 | — |
Reaction Steps
A mixture of 4-(5-bromo-2-hydroxy-phenylethynyl)-piperidine-1-carboxylic acid tert-butyl ester (70 mg), copper iodide (9 mg), N,N-dimethylformamide (1 mL), triethylamine (100 μL), and Pd(PPh3)2Cl2 (7 mg) is heated under an argon atmosphere to 55° C. for 0.5 h. The reaction mixture is diluted with ice water after cooling to room temperature and extracted with ethyl acetate. The combined extracts are dried over MgSO4 and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 80:20→50:50) to give the title compound. LC (method 2): tR=1.49 min; Mass spectrum (ESI+): m/z=380, 382 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853239B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-06141d448c0446f8be625e6d0f70c464 |
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| Source note | uspto-grants-2014_10 |
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