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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 705186Erstellt: 23. Oktober 2026

3',5'-Difluoroacetophenone → 2-(3,5-Difluorophenyl)propan-2-ol

https://huagongshe.com/de/reaction/705186

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3',5'-DifluoroacetophenoneHCID 518596—
EduktHCID 178418573HCID 178418573—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3,5-Difluorophenyl)propan-2-olHCID 57732159—

Reaktionsschritte

To a solution of 1-(3,5-difluorophenyl)ethanone (1.0 equiv) in THF (0.2 M) at 0° C. was added methylmagnesium bromide (1.0 M in THF, 1.15 equiv). After stirring for 4 hours the reaction was quenched by addition of NH4Cl(sat), diluted with EtOAc, washed with NaCl(sat), dried over MgSO4, filtered, concentrated and purified by ISCO SiO2 chromatography to yield 2-(3,5-difluorophenyl)propan-2-ol. To a solution of 2-(3,5-difluorophenyl)propan-2-ol in CH2Cl2 (0.1 M) at 0° C. was added 2,6 lutidine (6 equiv.) and than triisopropylsilyl trifluoromethanesulfonate (3.0 equiv.). After stirring for 3 hours at 0° C. and six hours at rt the solution was partitioned between EtOAc and NaHCO3(sat), separated, washed with NaCl(sat), dried over MgSO4, filtered, concentrated and purified by ISCO SiO2 chromatography to yield (2-(3,5-difluorophenyl)propan-2-yloxy)triisopropylsilane. (400 MHz, <cdcl3>) δ ppm 1.05-1.08 (m, 21 H) 1.57 (s, 6 H) 6.63 (s, 1 H) 7.00 (dd, J=9.39, 2.35 Hz, 2 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09173883B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-044e148c4ab54996ba08bcc06ca37a6f
Quellennotizuspto-grants-2015_11