HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indole, 1-ethyl-2-methyl- → 5-(2-methyl-3-indolyl)-5-(1-ethyl-2-methyl-3-indolyl)3,4-dichloro-2(5H)-furanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indole, 1-ethyl-2-methyl- | HCID 170432 | — |
| Reactant | 4-(2-Methyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid | HCID 236200 | — |
| Product | 5-(2-methyl-3-indolyl)-5-(1-ethyl-2-methyl-3-indolyl)3,4-dichloro-2(5H)-furanone | HCID 20442712 | — |
Reaction Steps
Following a procedure similar to that described above in Example 25, part B, 5.0 g (0.017 mole) of 4-(2-methyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid and 2.7 g (0.017 mole) of 1-ethyl-2-methylindole were interacted to obtain 5-(2-methyl-3-indolyl)-5-(1-ethyl-2-methyl-3-indolyl)-3,4-dichloro-2(5H)-furanone (Formula V: R=Y=Y1 =H; R1 =R3 =CH3 ; R2 =CH3CH2) as a red-blue solid which melted in the range of 282°-285° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04477676 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-e7aec54333d344719d703ac53bc8c233 |
| Source note | uspto-grants-1984_10 |