HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 404856Erstellt: 24. Oktober 2026
Dodecylbenzenesulphonic acid → 2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-ol
https://huagongshe.com/de/reaction/404856
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dodecylbenzenesulphonic acid | HCID 25457 | — |
| Edukt | 1-(4-Trifluoromethylphenyl)-2-(dimethylhydroxymethyl)-4-hydroxy-6,7-dimethoxynaphthalene | HCID 68855880 | — |
| Edukt | 3,4-Dimethoxyphenyl-2-(dimethylhydroxymethyl)-4-hydroxy-6-trifluoromethylnaphthalene | HCID 86619960 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-ol | HCID 67172141 | — |
Reaktionsschritte
The products from Step 4 (1-(4-trifluoromethylphenyl)-2-(dimethylhydroxymethyl)-4-hydroxy-6,7-dimethoxynaphthalene and 1-(3,4-dimethoxyphenyl-2-(dimethylhydroxymethyl)-4-hydroxy-6-trifluoromethylnaphthalene, 51.7 grams) were placed in a reaction flask equipped with a Dean-Stark trap and 775 mL of toluene was added. The reaction mixture was stirred under a nitrogen atmosphere and dodecylbenzene sulfonic acid (8.3 grams) was added. The reaction mixture was heated to reflux for 5 hours. Upon cooling to room temperature the reaction mixture was concentrated by rotary evaporation. The resulting brown solid was slurried in 300 mL of 15% ethyl acetate/85% hexanes. The solid was collected by vacuum filtration yielding 35.1 grams of 2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-ol. This material was not purified further but was used directly in the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08748634B2 |
|---|
| Quelldatensatz | uspto-grants-2014_06 |
|---|
| ORD ID | ord-d1c4b3dd9dc94c4ab28ce429096708c3 |
|---|
| Quellennotiz | uspto-grants-2014_06 |
|---|