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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247412Generated: November 2, 2026

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

https://huagongshe.com/reaction/2247412

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

t-Butyl N-(2-methoxybenzyl)carbamate (6.04 g) was dissolved in 50 ml of acetonitrile, and 4.6 g of N-bromosuccinimide was added thereto. The mixture was stirred at room temperature for 3 hours, and then 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 evaporated. The residue was washed with a mixed solvent of t-butyl methyl ether and hexane, to give 6.97 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687664B2
Source datasetuspto-grants-2010_03
ORD IDord-647d908904764a3f99f61637e9cb43fb
Source noteuspto-grants-2010_03