HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → 2-(2-Methyl-1-octyl-1H-indole-3-carbonyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 1H-Indole, 2-methyl-1-octyl- | HCID 170708 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(2-Methyl-1-octyl-1H-indole-3-carbonyl)benzoic acid | HCID 19763802 | 35.2% |
Reaction Steps
In a manner similar to that described in part A of Example 1 hereinabove, 7.4 g (0.05 mole) of phthalic anhydride, 16.0 g (0.053 mole) of 76.5 percent active 1-n-octyl-2-methylindole, and 13.3 g (0.1 mole) of aluminum chloride were interacted in 50 ml of benzene to obtain 6.9 g of 2-[(1-n-octyl-2-methyl-3-indolyl)carbonyl]benzoic acid (Formula VIII: R0 =R1 =R2 =R3 =Y1 =H; R5 =CH3 ; R6 =(CH2)7CH3), as a pink-colored powder which melted at 121°-123° C. The nuclear magnetic spectrum was in agreement with the structure and a significant maxima occurred at 1717 cm-1 (C=O; s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251446 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-1c401d14a77c4c0e9af4cb625a3b3fcd |
| Source note | uspto-grants-1981_02 |