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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1047391Erstellt: 26. Oktober 2026

Hydrochloric Acid → 2-Docosyloxy-9-(4-chlorophenyl)-9-fluorenol

https://huagongshe.com/reaction/1047391

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-Docosyloxy-9-fluorenoneHCID 66719005—
EduktHCID 178478191HCID 178478191—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Docosyloxy-9-(4-chlorophenyl)-9-fluorenolHCID 4692772288%

Reaktionsschritte

Under a nitrogen atmosphere, 2-docosyloxy-9-fluorenone (250 mg, 0.50 mmol) prepared in the above-mentioned 1-1 was suspended in THF (2.5 ml), and dissolved at 50° C. 4-Chlorophenylmagnesium bromide solution was added dropwise, and the mixture was stirred. After completion of the reaction, the reaction mixture was cooled to room temperature, 1N hydrochloric acid was added dropwise thereto in a water bath until foaming stopped to quench the reaction. The mixture was extracted with chloroform (15 ml), and washed 3 times with 1N hydrochloric acid (5 ml), 3 times with 5% NaHCO3 solution (5 ml), and once with 20% NaCl solution (5 ml). The organic layer was dried over Na2SO4, and the solvent of the filtrate was evaporated. The obtained residue was isolated and purified by silica gel column chromatography, and precipitated with methanol (3 ml) to give 2-docosyloxy-9-(4-chlorophenyl)-9-fluorenol (270 mg, 0.44 mmol, 88%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08569453B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-58aa747319a14635a26188dc5f11af86
Quellennotizuspto-grants-2013_10