HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844304Generated: October 27, 2026
N,N-Dimethylpropargylamine → HCID 54484834, compound
https://huagongshe.com/reaction/844304
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylpropargylamine | HCID 81643 | — |
| Reactant | tert-Butyl (3-chloro-4-iodophenyl)carbamate | HCID 22592440 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 54484834 | HCID 54484834 | — |
Reaction Steps
To a deoxygenated solution of (3-chloro-4-iodo-phenyl)-carbamic acid tert-butyl ester (10.0 g) in triethylamine (120 ml) is added 1-dimethylamino-2-propyne (2.82 g), bis(triphenyl-phosphine)palladium(II) chloride (0.4 g), and cuprous iodide (0.054 g). The mixture is stirred at room temperature under an atmosphere of argon for approximately 6 hours and is then heated briefly (ca. 10 minutes) to 60° C. The reaction mixture is then cooled, filtered through diatomaceous earth, and the solvent is removed by evaporation under reduced pressure. The residue is dissolved in ethyl acetate, washed three times with water, once with saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. The solvent is removed by evaporation under reduced pressure, and the residue is chromatographed over silica gel (80% ethyl acetate in hexanes is used as the eluant) to give the purified product as an amber oil that solidified on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380243B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-5994fed3119f4049ad00cd79bbfb2a2e |
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| Source note | uspto-grants-2002_04 |
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