HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904071Generated: October 30, 2026
N,N-Dimethylaniline → HCID 20463605, compound
https://huagongshe.com/reaction/1904071
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 3-[3-(Diethylamino)phenyl]-6-(dimethylamino)-2-benzofuran-1(3H)-one | HCID 20463586 | — |
| Solvent | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20463605 | HCID 20463605 | 68.7% |
Reaction Steps
33 g of 3-(m-diethylaminophenyl)-6-dimethylaminophthalide and 13 g of dimethylaniline were dissolved in 300 cc of tetrachloroethane. 14 g of anhydrous aluminum chloride was added to the solution, and then the mixture was heated at 50° C. for 3 hours with stirring. After the termination of reaction, 30% aqueous solution of caustic soda was added to the mixture to dissolve aluminum chloride while cooling with ice. Tetrachloroethane phase was steam distilled to remove unreacted dimethylaniline and tetrachloroethane. The remaining aqueous phase was neutralized with acetic acid to obtain a white solid. This solid was dissolved in 600 cc of 2.5% aqueous solution of caustic soda, and then heated at 50° C. 600 cc of 5% aqueous solution of potassium persulfate was added dropwise to the above solution, and then the mixture was heated at 60° C. for 3 hours. After the termination of reaction, the resultant precipitates were filtered and recrystallized from methanol to obtain 31 g of 3-(m-diethylaminophenyl)-3-(p-dimethylaminophenyl)- 6-dimethylaminophthalide having the following structure whose m.p. was 177°-178° C. in the form of colourless crystals. This compound become green on contact with silica gel. ##STR73##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04439610 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-8fcb9a7dce5f4a7c998f4ca89666d921 |
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| Source note | uspto-grants-1984_03 |
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