Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181652Generated: November 2, 2026

Methyl iodide → tert-Butyl 3-bromobenzyl(methyl)carbamate

https://huagongshe.com/reaction/1181652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 3-bromobenzylcarbamateHCID 11033439—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 3-bromobenzyl(methyl)carbamateHCID 20738487113.6%

Reaction Steps

19 g (475 mmol) of sodium hydride (60% in oil) are added portionwise to a solution of 128 g (447 mmol) of tert-butyl (3-bromobenzyl)carbamate in 800 ml of DMF, and the reaction medium is stirred until the evolution of gas has ceased. 29.3 ml (470 mmol) of methyl iodide are added dropwise and stirring is continued for 18 hours. The reaction medium is poured into ice-cold water and extracted with ethyl acetate. The organic phase is separated out by settling of the phases, dried over magnesium sulfate and evaporated. 152.5 g of tert-butyl (3-bromobenzyl)-N-methylcarbamate are obtained in a yield of 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285568B2
Source datasetuspto-grants-2007_10
ORD IDord-d20194bb04e44a5984fbdec8e481e0b2
Source noteuspto-grants-2007_10