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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536350Generated: October 31, 2026

Methyl iodide → 1-(((Tert-butoxy)carbonyl)(methyl)amino)cyclopropane-1-carboxylic acid

https://huagongshe.com/reaction/536350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acidHCID 688396—
SolventDimethylformamideHCID 6228—
Product1-(((Tert-butoxy)carbonyl)(methyl)amino)cyclopropane-1-carboxylic acidHCID 14358262—

Reaction Steps

To a solution of 1-(tert-butoxycarbonylamino)cyclopropanecarboxylic acid (201 mg, 1.0 mmol) in DMF (2 mL) was added NaH (120 mg, 3.0 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 10 min. before the addition of MeI (568 mg, 4.0 mmol). The mixture was then warmed up to room temperature and stirred for 2 hr. Saturated NH4Cl aqueous solution (20 mL) was added into the mixture, and the solution was extracted with EtOAc (3×10 mL). The combined organic layers were concentrated and the residue was dissolved in MeOH (3 ml) with NaOH (3 N, 1 mL). This mixture was stirred at 80° C. for 1 hr and cooled down to room temperature. The clear solution was purified directly on preparative RP-HPLC to provide 1-(tert-butoxycarbonyl(methyl)amino)cyclopropanecarboxylic acid. ESMS m/z 238.2 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859574B2
Source datasetuspto-grants-2014_10
ORD IDord-622c817e18584328bd3505a79691ce86
Source noteuspto-grants-2014_10