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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792292Generated: October 31, 2026

N-bromobutanimide → 1-(Bromomethyl)-3,5-di-tert-butylbenzene

https://huagongshe.com/reaction/1792292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3,5-Bis(tert-butyl)tolueneHCID 84819—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product1-(Bromomethyl)-3,5-di-tert-butylbenzeneHCID 444750761.2%

Reaction Steps

3,5-Bis(t-butyl)-1-methylbenzene (200 mg, 0.98 mmol) was dissolved in carbon tetrachloride (4 ml), and then N-bromosuccinimide (192 mg, 1.08 mmol) and AIBN (α,α′-azabisisobutyronitrile) (2 mg) were added thereto. The mixture was heated under reflux and stirred for 5 hours. The filtrate obtained from the filtration of the reaction mixture was evaporated under reduced pressure to give 170 mg (yield: 61%) of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074819B2
Source datasetuspto-grants-2006_07
ORD IDord-590bd6cc73ae45b885ec4d481e80acdd
Source noteuspto-grants-2006_07