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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707381Generated: October 31, 2026

Tert-Butylamine → 4-bromo-N-tert-butylbenzamide

https://huagongshe.com/reaction/1707381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant4-Bromobenzoyl chlorideHCID 68515—
SolventDichloromethaneHCID 6344—
Product4-bromo-N-tert-butylbenzamideHCID 603258—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 22.5 l of methylene chloride and 3030 ml of tert-butylamine is cooled to 0° C. Then a solution of 3 kg of 4-bromo-benzoyl chloride in 15 l of methylene chloride is added in portions. The mixture is cooled to 0°-5° C. and then stirred over night at room temperature. The reaction mixture is filtered and the filtrate washed with 5 l of methylene chloride, three times with 5 l of 3 N HCl, twice with 4 l of NaHCO3 and twice with 2 l of brine. The organic layer is dried over Na2SO4 and evaporated. The crude crystals are stirred with 8 l of ether for 30 minutes and the mixture is cooled to 0° C. and filtered. Thus 4-bromo-N-tert-butyl-benzamide is obtained in form of white crystals, m.p.133°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352795
Source datasetuspto-grants-1994_10
ORD IDord-b4ba48bdfb884b238b6d01e59ae2f109
Source noteuspto-grants-1994_10