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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592969Generated: October 30, 2026

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

https://huagongshe.com/reaction/1592969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 3-bromobenzylcarbamateHCID 11033439—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 3-bromobenzyl(methyl)carbamateHCID 20738487—

Reaction Steps

128 g (447 mmol) of tert-butyl (3-bromobenzyl)carbamate and 800 ml of DMF are introduced into a round-bottomed flask and under a nitrogen stream. 19 g (475 mmol) of sodium hydride (60% in oil) are added in small quantities and the mixture is stirred until the gas emission ceases. 29.3 ml (470 mmol) of methyl iodide are then added and the mixture is stirred overnight. The reaction medium is poured into ice-cold water, extracted with ethyl acetate, the organic phase decanted off, dried over magnesium sulphate and evaporated off. 152.5 g (92%) of the expected product are recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294639B2
Source datasetuspto-grants-2007_11
ORD IDord-3397b448857f49ebaf9dbdecc2995024
Source noteuspto-grants-2007_11