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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130348Erstellt: 24. Oktober 2026

Ammonium Chloride → (3-(1,3-Dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-ol

https://huagongshe.com/de/reaction/130348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt3-(Trifluoromethyl)benzaldehydeHCID 67990—
Edukt2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(3-(1,3-Dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-olHCID 69255414—

Reaktionsschritte

A 1.0 mL aliquot of 2-(3-bromophenyl)-1,3-dioxolane is added into magnesium (610 mg; 25 mmol) and THF (5 mL) under Argon. After the reaction is started, the residue of 2-(3-bromophenyl)-1,3-dioxolane (total: 5.73 g; 25 mmol) in THF (20 mL) is added dropwise into the reaction mixture. The resulting solution is stirred at room temp for six hours, and then at 50-60° C. for 20 hours. After the mixture is cooled, a solution of 3-(trifluoromethyl)-benzaldehyde (4.35 g; 25 mmol) in THF (20 mL) is added dropwise and the reaction is stirred at room temp for 24 hours. A saturated solution of NH4Cl (50 mL) is added and stirred for 30 minutes. The organic layer is separated and the aqueous layer is extracted with ethyl acetate (2×100 mL). The organic layers are combined and dried over anhydrous Na2SO4. The solvent is removed and the residue is purified by column chromatography on silica gel. Eluting with ethyl acetate/hexanes (20:80) provide a colorless oil (3.23 g; 40%) as (3-(1,3-dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-ol: MS 307.0 (M−17).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381736B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-d5bd1ef900304afea4d5fb5210705be1
Quellennotizuspto-grants-2008_06