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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430974Generated: October 30, 2026

Methyl iodide → Tert-butyl 2-(2-azidoethoxy)ethyl(methyl)carbamate

https://huagongshe.com/reaction/430974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl (2-(2-azidoethoxy)ethyl)carbamateHCID 12106197—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2-(2-azidoethoxy)ethyl(methyl)carbamateHCID 2109375694.2%

Reaction Steps

Sodium hydride (60% oil dispersion, 9.1 g, 228 mmol) was placed in a round bottom flask and washed with hexanes (3×) under N2. The dried sodium hydride was treated with 800 mL of anhydrous THF. A solution of tert-butyl 2-(2-azidoethoxy)ethylcarbamate (41.9 g, 182 mmol) in 200 mL of THF was then added to the stirred sodium hydride solution over 40 min. After addition was complete, the reaction was stirred an additional 20 min followed by addition of methyl iodide (13.6 mL, 218 mmol). After stirring overnight, the reaction was quenched with 300 mL of saturated NaHCO3 solution. The reaction mixture was then treated with 200 mL of H2O and 1 L of Et2O. The organic phase was separated and washed with H2O and brine. The organic portion was then dried over MgSO4 and concentrated under reduced pressure to give 41.9 g of tert-butyl 2-(2-azidoethoxy)ethyl(methyl)carbamate as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06656938B2
Source datasetuspto-grants-2003_12
ORD IDord-be28e82cdaf9407f9072a6dc9d935d3f
Source noteuspto-grants-2003_12