HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052228Generated: October 25, 2026
Methyl iodide → Methyl 2-((tert-butoxycarbonyl)amino)pent-4-enoate
https://huagongshe.com/reaction/1052228
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-{[(Tert-butoxy)carbonyl]amino}pent-4-enoic acid | HCID 5166119 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-((tert-butoxycarbonyl)amino)pent-4-enoate | HCID 10857232 | 98.6% |
Reaction Steps
A mixture of 2-[(tert-butoxycarbonyl)amino]pent-4-enoic acid (20.0 g), potassium carbonate (13.2 g) and N,N-dimethylformamide (100 mL) was stirred for 15 min. The mixture was cooled to 0° C., iodomethane (9.2 g) was added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was filtered, and the residue was washed with ethyl acetate. The filtrate was successively washed with 5% hydrochloric acid and brine, and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (21.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388195B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-c772f0111cc14430aac366327db83f57 |
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| Source note | uspto-grants-2016_07 |
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