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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855161Generated: October 31, 2026

Methyl iodide → 4-[[(1,1-dimethylethoxy)carbonyl]amino]Butanoic acid methyl ester

https://huagongshe.com/reaction/1855161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(((Tert-butoxy)carbonyl)amino)butanoic acidHCID 294894—
SolventAcetoneHCID 180—
Product4-[[(1,1-dimethylethoxy)carbonyl]amino]Butanoic acid methyl esterHCID 1311235283%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 4-(tert-butoxycarbonylamino)butanoic acid (7.0 g, 34.5 mmol) and K2CO3 (9.5 g, 68.9 mmol) in acetone (70 mL) was added MeI (7.5 g, 51.8 mmol) at rt. The reaction solution was stirred at 45° C. for 12 hrs. The mixture was washed with water and saturated sodium chloride, dried over Na2SO4, and concentrated to afford methyl 4-(tert-butoxycarbonylamino)butanoate (6.2 g, 83%) as a yellow oil. ESI-MS (EI+, m/z): 240 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962843B2
Source datasetuspto-grants-2015_02
ORD IDord-9124ed42664640ca8f6717ad8bc9db5a
Source noteuspto-grants-2015_02