HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-tert-Butyl-4-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-tert-Butyl-4-methylbenzamide | HCID 576940 | 89% |
Reaction Steps
The preparation of Example 1 was repeated with the changes that the starting reactants were tert-butyl amine (4.72 g, 0.065 mole) and 4-methylbenzoyl chloride (5.02 g, 0.0325 mole), the reaction was carried out in benzene and the reaction produced 5.54 g of crystals of the desired product (89% yield), mp 114°-116° C. Proton nuclear magnetic resonance (89.55 MHz) showed absorptions at 7.615 ppm (d, 8 Hz, 2H; 2,6-aryl H); 7.193 ppm (d, 8 Hz, 2H; 3.5-aryl H); 5.970 ppm (bs, 1H; N-H); 2.377 ppm (s, 3H; 4-CH3); 1.461 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-89e462aaeb1f494898bf5041cd2ed561 |
| Source note | uspto-grants-1995_12 |