HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20068379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20068400 | HCID 20068400 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20068379 | HCID 20068379 | 60.6% |
Reaction Steps
To a stirred mixture of 5.1 parts of 1-(1,2,3,4-tetrahydro-2,2-dimethyl-1-naphthalenyl)-1H-imidazole-5-methanamine and 75 parts of trichloromethane was added dropwise a solution of 2.0 parts of acetic acid anhydride in 150 parts of trichloromethane. Upon complete addition, stirring was continued for 1 hour at room temperature. The reaction mixture was washed with a sodium carbonate solution 10% and water, dried, filtered and evaporated. The residue was crystallized from 2-propanone. The product was filtered off and dried, yielding 3.61 parts (60.6%) of N-[[1-(1,2,3,4-tetrahydro-2,2-dimethyl-1-naphthalenyl)-1H-imidazol-5-yl]methyl]acetamide; mp. 166.3° C. (compound 2.47).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994103 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-41afafd709e84a2b9c5f063f7d05c135 |
| Source note | uspto-grants-1991_02 |