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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264385Generated: October 31, 2026

Methyl iodide → HCID 70003859, compound

https://huagongshe.com/reaction/1264385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 70000907HCID 70000907—
SolventDimethylformamideHCID 6228—
ProductHCID 70003859HCID 7000385977%

Reaction Steps

Under argon to 1.23 g (3.6 mmol) [[(4-Hydroxymethyl-phenyl)-methyl-carbamoyl]-methyl]-methyl-carbamic acid benzyl ester in 40 ml DMF were added 580 mg (13.3 mmol, 3.7 eq, 55% disp) sodium hydride, followed by 3.8 ml (59.6 mmol, 16.6 eq) methyl iodide. The suspension was stirred at RT over night, and added to ice water. The layers were separated and the inorganic one was extracted with 50 ml CH2Cl2 (3×). The combined organic layers were washed with water (2×), dried over MgSO4, filtered and evaporated. Column chromatography on silica gel with a gradient of CH2Cl2/MeOH (100:0-98:2) afforded 0.984 g (77%) [[(4-Methoxymethyl-phenyl)-methyl-carbamoyl]-methyl]-methyl-carbamic acid benzyl ester as a light yellow oil (Rf 0.07 CH2Cl2:MeOH 9:1), MS: 356 (M), +), which was deprotected according to 6.1. to give N-(4-Methoxymethyl-phenyl)-N-methyl-2-methylamino-acetamide as yellow oil (Rf 0.2 CH2Cl2:MeOH 9:1), MS: 223 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541638B2
Source datasetuspto-grants-2003_04
ORD IDord-70774c602a724577bf89e35eb22a3d3e
Source noteuspto-grants-2003_04