HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892213Generated: October 30, 2026
tert-butyl N-(prop-2-yn-1-yl)carbamate → HCID 70881450, compound
https://huagongshe.com/reaction/1892213
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl N-(prop-2-yn-1-yl)carbamate | HCID 11073648 | — |
| Reactant | 5-Bromo-2-methyl-3-nitropyridine | HCID 25067266 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | HCID 70881450 | HCID 70881450 | 79.3% |
Reaction Steps
To a solution of 5-bromo-2-methyl-3-nitropyridine (2.81 g, 12.9 mmol) in TEA (25 mL) was added tert-butyl prop-2-yn-1-ylcarbamate (2.58 g, 16.6 mmol). The solution was degassed with argon. To the reaction mixture were added bis(triphenylphosphine)palladium(II) chloride (0.18 g, 0.26 mmol) and copper(I) iodide (0.098 g, 0.52 mmol). The reaction mixture was allowed to stir at 70° C. for 2.5 h and was then concentrated and diluted with EtOAc (100 mL). The mixture was filtered over a pad of Celite® and the resulting filtrate was washed with sat. aq. NaHCO3 (100 mL). The organic solution was dried over MgSO4, filtered and concentrated. The residue was purified by column chromatography to give tert-butyl[3-(6-methyl-5-nitropyridin-3-yl)prop-2-yn-1-yl]carbamate (2.98 g, 79%) as a yellow solid. LCMS (FA): Rt=1.81 min, m/z=292.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507667B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-3723b5e38fd34dd59a4bfe3c070f664a |
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| Source note | uspto-grants-2013_08 |
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