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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442747Generated: November 2, 2026

Methyl iodide → tert-butyl N-[(4-bromophenyl)methyl]-N-methylcarbamate

https://huagongshe.com/reaction/1442747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactanttert-butyl N-[(4-bromophenyl)methyl]carbamateHCID 12453839—
SolventDimethylformamideHCID 6228—
Producttert-butyl N-[(4-bromophenyl)methyl]-N-methylcarbamateHCID 5916608299.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a 60-mL vial, tert-butyl-4-bromobenzylcarbamate (1.25 g, 4.37 mmol) was dissolved in DMF (12 mL). To this solution was added Ag2O (4.0 g, 17 mmol) followed by the addition of CH3I (0.68 mL, 11 mmol). The mixture was stirred at 50° C. for 18 hours. The reaction mixture was filtered through a bed of celite and the celite was washed with methanol (2×20 mL) and dichloromethane (2×20 mL). The filtrate was concentrated to remove most of the DMF. The residue was treated with water (50 mL) and a white emulsion formed. This mixture was extracted with ethyl acetate (4×25 mL), dried over Na2SO4, and the solvent was evaporated to yield tert-butyl-4-bromobenzyl(methyl)carbamate (1.3 g, 98%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659268B2
Source datasetuspto-grants-2010_02
ORD IDord-7f2a532b69794498ad409e401a5e8b70
Source noteuspto-grants-2010_02