Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDodecylbenzenesulphonic acidHCID 25457—
Reactant1-(4-Trifluoromethylphenyl)-2-(dimethylhydroxymethyl)-4-hydroxy-6,7-dimethoxynaphthaleneHCID 68855880—
Reactant3,4-Dimethoxyphenyl-2-(dimethylhydroxymethyl)-4-hydroxy-6-trifluoromethylnaphthaleneHCID 86619960—
SolventTolueneHCID 1140—
Product2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006427B2
Source datasetuspto-grants-2015_04
ORD IDord-122fad19cc6c4af88ced268d3e735447
Source noteuspto-grants-2015_04