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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245432Generated: November 3, 2026

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

https://huagongshe.com/reaction/1245432

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 after settling has taken place, 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 numberUS07125869B2
Source datasetuspto-grants-2006_10
ORD IDord-b2cdb92b08724e5aaf635c623f1b0c1b
Source noteuspto-grants-2006_10