Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296216Generated: October 25, 2026

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

https://huagongshe.com/reaction/1296216

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244861B2
Source datasetuspto-grants-2007_07
ORD IDord-52512523871d4e4d8e460cff3db66c96
Source noteuspto-grants-2007_07