HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 734471Erstellt: 24. Oktober 2026
Triethylamine → (1-Benzyl-1H-imidazol-2-yl)(2,3-dimethylphenyl)methanone
https://huagongshe.com/de/reaction/734471
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1-Benzylimidazole | HCID 77918 | — |
| Edukt | 2,3-Dimethylbenzoyl chloride | HCID 2800899 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (1-Benzyl-1H-imidazol-2-yl)(2,3-dimethylphenyl)methanone | HCID 66771502 | 91,3% |
Reaktionsschritte
To a solution of 1-benzyl-1H-imidazole (1.69 Kg, 10.56 mol) in dichloromethane (14.0 L), at −7° C., was added triethylamine (1.61 kg, 10.56 mol). A solution of 2,3-dimethylbenzoyl chloride (2.0 kg, 11.99 mol) in dichloromethane (6.0 L) was then added dropwise and the reaction mixture was stirred at room temperature for 16 h. The reaction was monitored by Thin layer Chromatography. After completion of the reaction, the reaction mixture was diluted with water (5.0 L) and the mixture was stirred for a further 15 min. The two layers were separated and the organic phase was concentrated in vacuo. To the residue was added toluene (8.0 L) and the solution was cooled to −5° C., before addition of hydrochloric acid (5N, 8.0 L). The two layers were separated and the aqueous layer was adjusted to pH 9-12, by addition of aqueous sodium hydroxide solution (50%), and extracted with toluene (4.0 L and then 8.0 L). The combined organic phases were concentrated in vacuo to give the title compound (2.8 kg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07592362B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-5a22b26a7f354c30a866bb816d169569 |
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| Quellennotiz | uspto-grants-2009_09 |
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