HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 12248790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 2-Methyl-5-nitro-1H-indole | HCID 280313 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 12248790 | HCID 12248790 | — |
Reaction Steps
Proceeding in a manner similar to that described in part A of Example 10, 29.6 g (0.20 mole) of phthalic anhydride and 35.2 g (0.20 mole) of 5-nitro-2-methylindole were interacted in 100 ml of ethylene dichloride to obtain 2-[(2-methyl-5-nitro-3-indolyl)carbonyl]benzoic acid (Formula VIII: Ro =R1 =R2 =R3 =R6 =H; R5 =CH3 ; Y1 =5-NO2), a red brown solid melting at 144°-148° C. and showing a strong carbonyl absorption maximum at 1700 cm-1 in the infrared spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307018 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-2559d2ffc0d8478ea948b51d8b7b8ab9 |
| Source note | uspto-grants-1981_12 |