HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 13561342, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Indole-2-carboxylic acid | HCID 72899 | — |
| Reactant | [(Phenyl)(4-dimethylaminophenyl)(4-methylphenylsulfonyl)]methane | HCID 20184822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13561342 | HCID 13561342 | — |
Reaction Steps
Proceeding in a manner similar to that described in Example 2 above, 20.5 g of [(phenyl)(4-dimethylaminophenyl)(4-methylphenylsulfonyl)]methane was interacted with 10.0 g of indole-2-carboxylic acid in the presence of 5.6 ml of concentrated hydrochloric acid in 140.0 ml of ethanol to obtain 3.34 g of [(phenyl)(4-dimethylaminophenyl)(2-carboxyindol-3-yl]methane (Formula XI: R1 =R2 =R3 =R4 =R11 =B"=H; R5 =N(CH3)2), a blue solid which melted at 213°-215° C. The nuclear magnetic resonance spectrum was consistent with the assigned structure. A toluene solution of the product spotted on an acid clay-coated paper slowly developed a purple-colored image and on a phenolic resin-coated paper slowly developed a dark blue-colored image.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04697018 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-754fa825e3b54d9da275dc1f88c648ce |
| Source note | uspto-grants-1987_09 |