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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005471Generated: October 26, 2026

N-bromobutanimide → Phenyl N-Methoxy-N-(2-bromomethylphenyl)carbamate

https://huagongshe.com/reaction/1005471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantphenyl N-methoxy-N-(2-methylphenyl)carbamateHCID 15767250—
CatalystN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
ProductPhenyl N-Methoxy-N-(2-bromomethylphenyl)carbamateHCID 2119183068.6%

Reaction Steps

A mixture of 324 g (1.3 mol) of phenyl N-methoxy-N-(2-methylphenyl)carbamate (Example 2b), 258 g (1.45 mol) of N-bromosuccinimide and 1 g of azoisobutyronitrile in 1 l of CCl4 is irradiated using a 300 W UV lamp for about 6 hours, whereby the reaction mixture is heated to boiling. 13 g of N-bromosuccinimide are then added and the mixture is irradiated for a further 8 hours. It is then cooled to room temperature and the precipitated succinimide is filtered off. The organic phase is then extracted with water, dried over MgSO4 and concentrated. The residue crystallizes and is stirred with cyclohexane. 300 g (68%) of the title compound are obtained as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054592
Source datasetuspto-grants-2000_04
ORD IDord-dfc67bdf67cb42f78fec3c178f30de5d
Source noteuspto-grants-2000_04