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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816582Generated: October 25, 2026

N-bromobutanimide → Tert-butyl (5-bromo-2-methoxybenzyl)carbamate

https://huagongshe.com/reaction/1816582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantTert-butyl (2-methoxybenzyl)carbamateHCID 22926021—
SolventAcetonitrileHCID 6342—
ProductTert-butyl (5-bromo-2-methoxybenzyl)carbamateHCID 2292603086.6%

Reaction Steps

6.04 g of tertiary butyl N-(2-methoxybenzyl)carbamate was dissolved in 50 ml acetonitrile, followed by adding 4.6 g of N-bromosuccinimide thereto. After stirring at room temperature for 3 hours, the solvent was evaporated. The residue was dissolved in ethyl acetate and successively-washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evapoarated. The residue was washed with a mixture of methyl tertiary butyl methyl ether and hexane, to give 6.97 g of tertiary butyl N-(5-bromo-2-methoxybenzyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884821B1
Source datasetuspto-grants-2005_04
ORD IDord-f64ec6f64a6e490089b7f086cb208991
Source noteuspto-grants-2005_04