HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethylindole → 4-(1,2-Dimethyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethylindole | HCID 13408 | — |
| Reactant | Dichloromaleic anhydride | HCID 70728 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(1,2-Dimethyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid | HCID 236202 | 91.5% |
Reaction Steps
A mixture of 10.0 g (0.07 mole) of 1,2-dimethylindole, 12.0 g (0.07 mole) of dichloromaleic anhydride and 200 ml of ethylene dichloride was stirred at ambient temperature for approximately eighteen hours. The solid present in the reaction mixture was collected by filtration. After drying at 60° C in vacuo there was obtained 20.0 g of 4-(1,2-dimethyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid (Formula VIII: R=R1 =CH3 ; Y=H) as a pale blue solid which melted over the range 150° to 153° C. Infrared spectral analysis showed a maximum at 1712 (C=0; s) cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075224 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-281d4c2a1f874541998c68024388dc13 |
| Source note | uspto-grants-1978_02 |