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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426484Generated: October 31, 2026

Methyl iodide → Methyl 2-((tert-butoxycarbonyl)amino)pent-4-enoate

https://huagongshe.com/reaction/1426484

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 numberUS08933069B2
Source datasetuspto-grants-2015_01
ORD IDord-c410c51fc3bb47dd87343953fba53335
Source noteuspto-grants-2015_01