HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, (triethoxymethyl)- → 1-Acetyl-3-(1-ethoxy-1-phenylmethylidene}-2-indolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, (triethoxymethyl)- | HCID 74268 | — |
| Reactant | 1-Acetylindolin-2-one | HCID 323719 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 1-Acetyl-3-(1-ethoxy-1-phenylmethylidene}-2-indolinone | HCID 54237888 | — |
Reaction Steps
35.0 g (0.2 mol) of 1-acetyl-2-indolinone are dissolved in 300 ml of acetic anhydride and after the addition of 135 g (0.6 mol) of triethyl orthobenzoate the mixture is refluxed for 22 hours. The solvent is distilled off and the residue diluted with petroleum ether. After 18 hours' standing at ambient temperature, the crystalline precipitate is suction filtered, washed and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855710B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-9cad90a0f5794d64b7d4ec75067742a0 |
| Source note | uspto-grants-2005_02 |