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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541143Generated: October 25, 2026

Sodium Bicarbonate → methyl 9-hydroxy-4-methyl-9-trifluoromethyl-9H-fluorene-2-carboxylate

https://huagongshe.com/reaction/541143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantLithium acetateHCID 3474584—
Reactantmethyl 4-methyl-9-oxo-9H-fluorene-2-carboxylateHCID 59492531—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Productmethyl 9-hydroxy-4-methyl-9-trifluoromethyl-9H-fluorene-2-carboxylateHCID 5949263478%

Reaction Steps

Under an argon atmosphere, methyl 4-methyl-9-oxo-9H-fluorene-2-carboxylate (1.009 g), trimethyl(trifluoromethyl)silane (0.89 ml) and dimethylformamide (50 ml) were mixed, lithium acetate (0.027 g) was added with stirring at room temperature, and the mixture was further stirred at room temperature for 30 min. Acetic acid (0.7 ml) and a 1M solution (6 ml) of tetrabutylammonium fluoride in tetrahydrofuran were added, and the mixture was further stirred at room temperature for 15 min. To the reaction mixture was added aqueous sodium hydrogen carbonate (300 ml), and the mixture was extracted twice with ethyl acetate (50 ml). The combined organic layer was washed once with saturated aqueous sodium hydrogen carbonate, 4 times with water and once with saturated brine, and concentrated under reduced pressure. To the obtained residue was added hexane/ethyl acetate (8:2, 10 ml) and the mixture was stirred for 10 min. This slurry was filtered, and the obtained solid was dried to give the title compound (1.000 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871934B2
Source datasetuspto-grants-2014_10
ORD IDord-e0cdcf5464f64c58a1507c5e5fc2197e
Source noteuspto-grants-2014_10