Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955251Generated: November 2, 2026

Methyl iodide → [5-(2-Benzyloxy-ethoxy)-2-nitro-phenyl]-methyl-carbamic acid methyl ester

https://huagongshe.com/reaction/1955251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant[5-(2-Benzyloxy-ethoxy)-2-nitro-phenyl]-carbamic acid methyl esterHCID 53935046—
SolventDimethylformamideHCID 6228—
Product[5-(2-Benzyloxy-ethoxy)-2-nitro-phenyl]-methyl-carbamic acid methyl esterHCID 5455554289%

Reaction Steps

To a solution of [5-(2-benzyloxy-ethoxy)-2-nitro-phenyl]-carbamic acid methyl ester (2.03 g, 5.86 mmol) in anhydrous dimethylformamide (20 ml) was added iodomethane (1.82 ml, 29.3 mmol), followed by portion wise addition of NaH (0.35 g, 60%, 8.79 mmol). The reaction was stirred under nitrogen for 2 h. The reaction was quenched with NH4Cl (sat) (10 ml) and brine (10 ml), and the aqueous layer was extracted with ether (3×30 ml). The combined organics were dried over MgSO4, filtered and evaporated. The residue was chromatographed on silica gel eluting with hexanes, then 30% ethyl acetate/hexanes to give [5-(2-benzyloxy-ethoxy)-2-nitro-phenyl]-methyl-carbamic acid methyl ester (0.93 g, 89%) as an oil. Analysis calculated for C18H20N2O6 : C, 59.99; H, 5.59; N, 7.77. Found: C, 59.30; H, 5.34; N, 7.62.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124323
Source datasetuspto-grants-2000_09
ORD IDord-2d6906aa0e4c491e9da7edaf8625f549
Source noteuspto-grants-2000_09