HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439501Generated: October 31, 2026
4-Butylaniline → Hexanamide, N-phenyl- (9CI)
https://huagongshe.com/reaction/1439501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Butylaniline | HCID 7694 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Water | HCID 962 | — |
| Product | Hexanamide, N-phenyl- (9CI) | HCID 12118 | — |
Reaction Steps
One hundred grams of I, 4-n-butylaniline, were stirred with 500 grams H2O and 410 grams acetic anhydride added all at once. The temperature rose spontaneously to 45° C. and was raised briefly to 85° C, to bring all the solids into solution. Slow cooling, filtration, and overnight air drying gave 117.4 grams (92%) white plates of II, 4-butylacetanilide, mp 104°-105° C. (lit.1, mp 107° C). This 117.4 grams II were stirred with 486 grams acetic anhydride and 284 ml. 71% HNO3 added at such a rate that, after a brief induction period and with ice cooling, the temperature was kept at 30°-35° C. The reaction mixture was stirred 30 minutes at 5° C, then 300 grams ice, followed by 600 ml. H2O were added and the yellow solid filtered, washed copiously with H2O, and air dried to give 129.9 grams (90%) bright yellow III, 4-butyl-2-nitroacetanilide, mp 71°-73° C (lit.1, mp 76° C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04060491 |
|---|
| Source dataset | uspto-grants-1977_11 |
|---|
| ORD ID | ord-8cbfbde81f104afda3f13b62fc800df7 |
|---|
| Source note | uspto-grants-1977_11 |
|---|