HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → 1-(3-Chlorophenyl)-3-(ethoxymethylene)-2(1H,3H)-indolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 1-(3-Chlorophenyl)-indolin-2-one | HCID 11299530 | — |
| Reactant | Orthoformate | HCID 21585117 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(3-Chlorophenyl)-3-(ethoxymethylene)-2(1H,3H)-indolone | HCID 53712643 | 140.1% |
Reaction Steps
1-(3-Chlorophenyl)-2(1H,3H)-indolone (2.4 g, 0.01 mole) and triethyl orthoformate (8.3 ml, 0.05 mole) were combined and heated at 150°±10° for 18 hours. An additional 20 ml of the orthoformate were added and heating continued 2 hours. The reaction mixture was cooled to 25°, diluted with ether, washed with H2O and then brine, dried over MgSO4, concentrated in vacuo to oily solids, and triturated with pentane to yield solids (4.2 g). The solids were chromatographed on silica gel (7.5×15 cm) with 4:1 hexane:ethyl acetate as eluant to yield purified title product, 0.5 g; m.p. 132°-134°; m/e 310/299.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04861880 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-9921661696c64a11afbb267a74da802d |
| Source note | uspto-grants-1989_08 |