HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871806Generated: November 1, 2026
2,6-Dimethylaniline → HCID 15285306, compound
https://huagongshe.com/reaction/1871806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dimethylaniline | HCID 6896 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 15285305 | HCID 15285305 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15285306 | HCID 15285306 | 32.2% |
Reaction Steps
To a stirred mixture of 400 mg of 5-chloro-3-(2-chlorophenyl)-1-benzothiophen-2-carboxylic acid and 0.27 cc of diphenylphosphoryl azide in 3 cc of benzene was added dropwise 0.175 cc of triethylamine at room temperature. The resulting mixture was stirred at room temperature for 15 minutes and then heated under reflux for 20 minutes. After cooling, 0.16 cc of 2,6-dimethylaniline was added and the resulting mixture was stirred at room temperature for 30 minutes, followed by refluxing for 1 hour. After cooling, water was added to the reaction mixture and was extracted with chloroform. The extract was dried over magnesium sulfate and distilled to remove the solvent. The crude product thus obtained was purified by a silica gel column chromatography (eluent: chloroform/hexane=7/3) to obtain 175 mg of compound 64.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE036832 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-f9f3a7a7859d4974b7e80d00d25ec902 |
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| Source note | uspto-grants-2000_08 |
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