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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976631Generated: October 25, 2026

Methyl iodide → tert-butyl N-benzyloxy-N-methylcarbamate

https://huagongshe.com/reaction/976631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl N-(benzyloxy)carbamateHCID 736159—
Reactanttert-butyl N-benzyloxy-N-(2-methylpropyl)carbamateHCID 19967428—
SolventDimethylformamideHCID 6228—
Producttert-butyl N-benzyloxy-N-methylcarbamateHCID 14227181—

Reaction Steps

Sodium hydride (0.48 g of 80% in mineral oil, 16 mmol) was added to a solution of tert-butyl N-benzyloxycarbamate (Compound 54 Part A, 3 g, 13 mmol) in N,N-dimethylformamide (25 mL). The reaction mixture was stirred for 20 minutes then iodomethane (1.1 mL, 18 mmol) was added dropwise with cooling in an ice bath. The resulting suspension was stirred at ambient temperature under a nitrogen atmosphere overnight. The reaction mixture was quenched with water (50 mL) then extracted with diethyl ether (150 mL). The organic layer was washed with water (5×50 mL), dried over magnesium sulfate then concentrated to provide 3.1 g of tert-butyl N-benzyloxy-N-methylcarbamate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612377
Source datasetuspto-grants-1997_03
ORD IDord-3b5ac8a5b1854f79944972dfbdf8fb6b
Source noteuspto-grants-1997_03