HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470205Generated: October 25, 2026
Dodecylbenzenesulphonic acid → 2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-ol
https://huagongshe.com/reaction/1470205
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dodecylbenzenesulphonic acid | HCID 25457 | — |
| Reactant | 1-(4-Trifluoromethylphenyl)-2-(dimethylhydroxymethyl)-4-hydroxy-6,7-dimethoxynaphthalene | HCID 68855880 | — |
| Reactant | 3,4-Dimethoxyphenyl-2-(dimethylhydroxymethyl)-4-hydroxy-6-trifluoromethylnaphthalene | HCID 86619960 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-ol | HCID 67172141 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006427B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-122fad19cc6c4af88ced268d3e735447 |
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| Source note | uspto-grants-2015_04 |
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