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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250818Generated: October 25, 2026

Methyl iodide → N-BOC-N-Methyl-3-bromoaniline

https://huagongshe.com/reaction/250818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantN-(tert-Butoxycarbonyl)-3-bromoanilineHCID 2757254—
SolventDimethylformamideHCID 6228—
ProductN-BOC-N-Methyl-3-bromoanilineHCID 2299714895%

Reaction Steps

To a solution of 114 g (447 mmol) of tert-butyl (3-bromophenyl)carbamate in 800 ml of DMF are added portionwise 19 g (475 mmol) of sodium hydride (60% in oil) 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 of the phases, dried over magnesium sulfate and evaporated. 115 g of tert-butyl (3-bromophenyl)-N-methylcarbamate are obtained in a yield of 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863332B2
Source datasetuspto-grants-2011_01
ORD IDord-9e174b4906214e0bad73be36a5c81fc0
Source noteuspto-grants-2011_01