HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 4-bromo-N-tert-butylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-bromo-N-tert-butylbenzamide | HCID 603258 | 89% |
Reaction Steps
The preparation of Example 1 was repeated with the changes that tert-butyl amine (4.02 g, 0.055 mole) and 4-bromobenzoyl chloride (6.04 g, 0.0275 mole) were the starting reactants and benzene was the reaction medium. This reaction produced 6.24 g crystals (89% yield), mp 130°-133° C. Proton nuclear magnetic resonance (89.55 MHz) showed absorptions at 7.562 ppm (s, 4H; aryl H); 5.910 ppm (bs, 1H; N-H); 1.464 ppm (s, 9H; tert-butyl H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05472983 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-ed9a7e7125504a419ad0ebc4531f49be |
| Source note | uspto-grants-1995_12 |