Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131277Generated: October 27, 2026

Methyl iodide → Methyl 4-(((tert-butoxycarbonyl)(methyl)amino)methyl)benzoate

https://huagongshe.com/reaction/131277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-((((1,1-dimethylethoxy)carbonyl)amino)methyl)benzoateHCID 14221817—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-(((tert-butoxycarbonyl)(methyl)amino)methyl)benzoateHCID 1778910794%

Reaction Steps

To a solution of methyl 4-[[(tert-butoxycarbonyl)amino]methyl]benzoate (compound obtained in Reference Example 81(1), 2.0 g) in tetrahydrofuran (20 mL) is added sodium hydride (60% dispersion in mineral oil, 0.9 g) under ice-cooling. The mixture is stirred at room temperature for 30 minutes and then to the reaction mixture is added dropwise methyl iodide (2.3 mL). The mixture is stirred at room temperature for 3 hours. The reaction mixture is diluted with ethyl acetate, washed with water, and concentrated in vacuo to give methyl 4-[[N-methyl-N-(tert-butoxycarbonyl)amino]-methyl]benzoate (1.9 g, yield; 94%) as a yellow oil. MS (APCI) m/z: 280 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384952B2
Source datasetuspto-grants-2008_06
ORD IDord-307dbef7c4144e9681d165ff89ba1cfc
Source noteuspto-grants-2008_06