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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-{[(Tert-butoxy)carbonyl]amino}pent-4-enoic acidHCID 5166119—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-((tert-butoxycarbonyl)amino)pent-4-enoateHCID 1085723298.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388195B2
Source datasetuspto-grants-2016_07
ORD IDord-c772f0111cc14430aac366327db83f57
Source noteuspto-grants-2016_07