HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-(6-Bromo-naphthalen-2-yl)-5-methyl-[1,2,4]oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178513225 | HCID 178513225 | — |
| Solvent | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Product | 3-(6-Bromo-naphthalen-2-yl)-5-methyl-[1,2,4]oxadiazole | HCID 59534075 | — |
Reaction Steps
6.11 ml acetic anhydride are added to 4.40 g 6-bromo-N-hydroxy-naphthalene-2-carboxamidine in 30 ml 2,4,6-trimethylpyridine. The reaction mixture is stirred for one hour at ambient temperature and then heated to 130° C. for four hours. After the reaction has ended the mixture is evaporated down in vacuo and the flask residue is stirred with ethyl acetate and petroleum ether, suction filtered and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163911B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-5ce417c6628c48d1804740330ea7b28a |
| Source note | uspto-grants-2012_04 |