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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581747Generated: October 25, 2026

N-bromobutanimide → 3-bromomethyl-2,4-dichloro-N-methyl-N-(phthalimidoacetyl)aniline

https://huagongshe.com/reaction/581747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile)HCID 85867—
Reactant2,6-dichloro-3-[N-(phthalimidoacetyl)-N-methylamino]tolueneHCID 22113013—
SolventDichloromethaneHCID 6344—
Product3-bromomethyl-2,4-dichloro-N-methyl-N-(phthalimidoacetyl)anilineHCID 2211333827.8%

Reaction Steps

A mixture of 2,6-dichloro-3-[N-(phthalimidoacetyl)-N-methylamino]toluene (303 mg), N-bromosuccinimide (150 mg), 2,2'-azobis-(2,4-dimethyl-4-methoxyvaleronitrile) (30 mg) and dichloromethane (6 ml) was heated under reflux for 5 hours. N-Bromosuccinimide (75 mg) was added therein and the mixture was heated under reflux for additional 3 hours. The reaction mixture was washed with saturated sodium bicarbonate solution twice and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was crystallized from diethyl ether to give 3-bromomethyl-2,4-dichloro-N-methyl-N-(phthalimidoacetyl)aniline (102 mg) as crystals. mp: 211° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922711
Source datasetuspto-grants-1999_07
ORD IDord-0dea4617883b498bbc4be403d81c099a
Source noteuspto-grants-1999_07