HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-tert-Butyl-4-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Product | N-tert-Butyl-4-nitrobenzamide | HCID 591441 | 77% |
Reaction Steps
The preparation of Example 1 was repeated with the changes that tert-butyl amine (14.6 g, 0.200 mole) and 4-nitrobenzoyl chloride (18.6 g, 0.100 mole) were the starting reactants. This reaction produced 17.13 g of crystals of the desired product (77% yield), mp 162°-163° C. proton nuclear magnetic resonance (89.55 MHz) showed absorptions at 8.257 ppm (d, 8.8 Hz, 2H; 3,5-aryl H); 7.878 ppm (d, 8.8 Hz, 2H; 2,6-aryl H); 6.097 ppm (bs, 1H; N-H); 1,500 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-d5a4b96c22c546fcb9cf020e91142f04 |
| Source note | uspto-grants-1995_12 |