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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985293Generated: October 25, 2026

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

https://huagongshe.com/reaction/1985293

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 was continued at room temperature for 3 hours, the solvent was evaporated. The residue was dissolved in ethyl acetate, and washed successively with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was washed with a mixed solution of methyl t-butyl ether and hexane, to give 6.97 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544835B2
Source datasetuspto-grants-2009_06
ORD IDord-7df243ff2a4f4008a919224b26af209b
Source noteuspto-grants-2009_06