HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[4-[1-(1H-imidazol-1-yl)ethyl]phenyl]formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 4-[1-(1H-imidazol-1-yl)ethyl]benzenamine | HCID 14518365 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | N-[4-[1-(1H-imidazol-1-yl)ethyl]phenyl]formamide | HCID 14518360 | 80% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
(a-4) To a stirred solution of 15 parts of 4-[1-(1H-imidazol-1-yl)ethyl]-benzenamine and 2.7 parts of sodium formate in 60 parts of formic acid is added dropwise a solution of 9 parts of acetic acid anhydride in 24 parts of formic acid at 50° C. The reaction mixture was stirred for 1 hour at 100° C. and the solvent was evaporated. The residue was dissolved in a small amount of ice water and the solution was treated with ammonium hydroxide while cooling. The product was extracted twice with dichloromethane. The combined extracts were dried, filtered and evaporated. The residue was crystallized twice from tetrahydrofuran, yielding 13.8 parts (80%) of N-[4-[1-(1H-imidazol-1-yl)ethyl]phenyl]-formamide; mp. 129.4° C. (int. 115).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04859684 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-7376947100e44175beb11a11710ceb16 |
| Source note | uspto-grants-1989_08 |