HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543029Generated: October 30, 2026
Acetic Anhydride → HCID 14149593, compound
https://huagongshe.com/reaction/543029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 15519329 | HCID 15519329 | — |
| Reactant | HCID 21284000 | HCID 21284000 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14149593 | HCID 14149593 | 37.1% |
Reaction Steps
A mixture of 14.5 g of 2-(2-methyl-4-dimethylaminophenyl)carbonylbenzoic acid, 11.5 g of 1-(2-ethoxyethyl)-2-methylindole and 40.0 ml acetic anhydride was maintained at approximately 70° C. for approximately four hours. The resulting solution was cooled to ambient temperature and slowly poured into a mixture of toluene and 5 percent aqueous ammonium hydroxide. The toluene layer was separated, washed with water and then with saturated sodium chloride solution. The toluene solution was evaporated to dryness. The residue which remained was recrystallized twice from a mixture of hexane and isopropyl alcohol to obtain 8.9 g of 3-[1-(2-ethoxyethyl)-2-methylindol-3-yl]-3-(2-methyl-4-dimethylaminophenyl)phthalide (Formula I: R=C2H5OC2H4 ; R1 =R2 =R3 =R4 =CH3 ; X=Y=H), a white-colored solid which melted at 170.5° to 171° C. Significant infrared maxima appeared at 1750 (C=O;s) and 1123 (C--O;s)cm-1. A toluene solution of the product spotted on an acid clay or a phenolic resin coated paper developed a cyan-colored image.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04660060 |
|---|
| Source dataset | uspto-grants-1987_04 |
|---|
| ORD ID | ord-8d7829aa13f8402b9fb1080b640d5639 |
|---|
| Source note | uspto-grants-1987_04 |
|---|