HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1,3-Indandione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl naphthalene-1,2-dicarboxylate | HCID 21894257 | — |
| Product | 1,3-Indandione | HCID 11815 | — |
Reaction Steps
To a 50% dispersion of sodium hydride in mineral oil (4.55 g) was added to a solution of diethyl naphthalene 1,2-dicarboxylate (18.5 g) in ethyl acetate (22 ml.) and the mixture refluxed for 3.5 hrs. on a steam bath. After cooling the precipitated orange solid was filtered and decarboxylated with hydrochloric acid (35 ml.) in water (350 ml) at 70°C over 7 mins. to yield benze(e) indane-1,3-dione, m.p. (benzene) 178°C (decomp.) (Found: C, 79.21; H, 4.22; C13H8O2 requires: C, 79.58; H, 4.11%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03978231 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-f88e3bab156f4465a3aef38a2429ebbc |
| Source note | uspto-grants-1976_08 |