HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721091Erstellt: 24. Oktober 2026
p,alpha-DIMETHYLBENZYL ALCOHOL → 1-(4-Methylphenyl)ethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamate
https://huagongshe.com/de/reaction/721091
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | p,alpha-DIMETHYLBENZYL ALCOHOL | HCID 10817 | — |
| Edukt | Triphosgene | HCID 94429 | — |
| Edukt | 4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylaniline | HCID 21890421 | — |
| Edukt | Toluene triethylamine | HCID 22504574 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-(4-Methylphenyl)ethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamate | HCID 21890036 | 73,3% |
Reaktionsschritte
4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline (80 mg) was added to toluene/triethylamine=10/1 (8 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (111 mg) in methylene chloride was then added to the solution, and the mixture was heated under reflux for 15 min. Subsequently, 4-methyl-α-methylbenzyl alcohol (50 mg) was added thereto, and the mixture was further stirred with heating under reflux for 2 hr. After the completion of the reaction, the reaction solution was allowed to cool to room temperature before distilled water was added thereto. The mixture was subjected to separatory extraction with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution and saturated brine. The washed solution was dried over sodium sulfate and was concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (88mg, yield 68%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07135466B2 |
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| Quelldatensatz | uspto-grants-2006_11 |
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| ORD ID | ord-f4d8cc99eb694ad49393c5bc975c7366 |
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| Quellennotiz | uspto-grants-2006_11 |
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