HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibromonaphthalic anhydride → Naphthalic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibromonaphthalic anhydride | HCID 87118624 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Naphthalic anhydride | HCID 6693 | — |
Reaction Steps
The following morning thin-layer chromatography showed only a trace presence of the dibromonaphthalic anhydride. The reaction mixture was cooled to room temperature followed by the addition of 350 ml of ether. The. triethylamine hydrobromide byproduct was removed by filtration. The filtrate was concentrated on the rotary evaporator, to give the diphenylethynyl derivative of the 1,8-naphthalic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063168B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-ee79eb69617e456a8906bb8d02ec4325 |
| Source note | uspto-grants-2011_11 |