HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(7-Methoxynaphthalen-1-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 2-(7-Methoxynaphthalen-1-yl)acetamide | HCID 15149127 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(7-Methoxynaphthalen-1-yl)acetonitrile | HCID 11264068 | — |
Reaction Steps
The (7-methoxynaphth-1-yl)acetamide obtained in Stage E is suspended in 80 ml of anhydrous THF, and triethylamine is added. The solution is cooled in an ice bath, and then trifluoroacetic anhydride is added dropwise with magnetic agitation. Agitation is continued for one hour at room temperature. Then the mixture is dried and the residue taken up in water. The precipitate which forms is spun down, dried and recrystallized in isopropyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225442 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-0d8297132e0147d980039df82d6e1541 |
| Source note | uspto-grants-1993_07 |