HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 11049111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 20089846 | HCID 20089846 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11049111 | HCID 11049111 | — |
Reaction Steps
1.65 mmol of 2,3-di-(trifluoromethyl)-naphthacene-5,12-dione, 5 ml of ethyl acetate, 4.96 mmol of potassium acetate and 3 ml of acetic anhydride are hydrogenated for 35 minutes at 20°-25° C., with the addition of 0.1 g of Pd/C (5%). The reaction mixture is filtered and the residue is washed three times with CH2Cl2. The filtrates are evaporated and the residue is recrystallized from CHCl2 /pentane. 2,3-Di-(trifluoromethyl)-5,12-diacetoxynaphthacene is obtained in a yield of 0.45 g (70%), melting point 149°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05011944 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-746b3aa10fbc408c96d4a5ac90429fff |
| Source note | uspto-grants-1991_04 |