HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indole, 1-ethyl-2-methyl- → HCID 20442778, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indole, 1-ethyl-2-methyl- | HCID 170432 | — |
| Reactant | HCID 54180223 | HCID 54180223 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20442778 | HCID 20442778 | — |
Reaction Steps
A mixture of 7.0 g (0.02 mole) of 4-(2-phenyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid (prepared in part A above), 3.5 g (0.02 mole) of 1-ethyl-2-methylindole and 200 ml of acetic anhydride was stirred at ambient temperature in an atmosphere of air for approximately seventeen hours. The pale blue solid that formed was collected by filtration and dried in vacuo at 60° C. to obtain 5-(2-phenyl-3-indolyl)-5-(1-ethyl-2-methyl-3-indolyl)-3,4-dichloro-2(5H)-furanone (Formula V: R=Y=Y1 =H; R1 =C6H5 ; R2 =CH3CH2 ; R3 =CH3) as a tan-colored solid which started to sinter at 213° C. and was completely melted at 225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377698 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-e0540021c070425bb766d79316ae2e46 |
| Source note | uspto-grants-1983_03 |