HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533109Generated: October 26, 2026
Triethylamine → 4-(5-Bromo-2-hydroxy-phenylethynyl)-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/533109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromo-2-iodophenol | HCID 10924532 | — |
| Reactant | tert-Butyl 4-ethynylpiperidine-1-carboxylate | HCID 15550481 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(5-Bromo-2-hydroxy-phenylethynyl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 86686877 | — |
Reaction Steps
A mixture of 4-ethynyl-piperidine-1-carboxylic acid tert-butyl ester (4.03 g), 4-bromo-2-iodo-phenol (5.00 g), Pd(PPh3)2Cl2 (600 mg), copper iodide (500 mg), and triethylamine (2.35 mL) in N,N-dimethylformamide (30 mL) is heated under an argon atmosphere to 75° C. for 4 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→60:40) to give the title compound. LC (method 2): tR=1.32 min; Mass spectrum (ESI+): m/z=402, 404 [M+Na]+.
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-3bf071de59db47d78f17ad6fcb8d0af7 |
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| Source note | uspto-grants-2014_10 |
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