HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrachlorophthalic anhydride → HCID 21284003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrachlorophthalic anhydride | HCID 8326 | — |
| Reactant | 1H-Indole, 1-(2-methoxyethyl)-2-methyl- | HCID 14149588 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21284003 | HCID 21284003 | 112% |
Reaction Steps
Proceeding in a manner similar to that described in part A of Example 8 above, 30.0 g of tetrachlorophthalic anhydride was interacted with 40.0 g of 1-(2-methoxyethyl)-2-methylindole in 75.0 ml of glacial acetic acid at approximately 110° C. for approximately one hour to obtain 55.83 g of 2-[1-(2-methoxyethyl)-2-methylindol-3-yl]carbonyl-3,4,5,6-tetrachlorobenzoic acid, (Formula V: R=CH3OC2H4 ; R1 =CH3 ; X=Cl4 ; Y=H), a pale yellow solid which melted at 182°-184° C. A significant infrared maximum appeared at 1750 (C=O; s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04736027 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-5df77ac4ae5941f1a21a5988a6b4bc8e |
| Source note | uspto-grants-1988_04 |