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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-bromo-N-tert-butylbenzamide | HCID 603258 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05352795 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-b4ba48bdfb884b238b6d01e59ae2f109 |
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| Source note | uspto-grants-1994_10 |
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