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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1180040Erstellt: 26. Oktober 2026

Trifluoroacetic acid → 4-[4-(2-Pyrrolidin-1-yl-ethoxy)-benzyl]-phenol

https://huagongshe.com/reaction/1180040

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktTriethylsilaneHCID 12052—
Eduktp-((Trimethylsilyl)oxy)benzaldehydeHCID 70536—
EduktN-(2-(p-bromophenoxy)ethyl)pyrrolidineHCID 70657—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[4-(2-Pyrrolidin-1-yl-ethoxy)-benzyl]-phenolHCID 2204796594,3%

Reaktionsschritte

To a stirred solution of 1-[2-(4-bromo-phenoxy)-ethyl]-pyrrolidine (2.89 g, 10.7 mmol) in THF (30 mL) was added dropwise 1.6 M solution in hexanes n-BuLi (7 mL, 10.2 mmol) over a 5-min period at −78° C. The mixture was stirred at −78° C. for 15 min before 4-trimethylsilyloxybenzaldehyde (2.08 g, 10.7 mmol) was added. The mixture was allowed to warm to rt during 20 min and quenched with water. Extraction with CH2Cl2, drying (MgSO4), filtration and evaporation provided the crude diarylmethanol which was dissolved in CH2Cl2 (30 mL) and stirred with triethylsilane (4 mL) and TFA (5 mL) for 16 h at rt. Evaporation gave 3.0 g (84%) 4-[4-(2-pyrrolidin-1-yl-ethoxy)-benzyl]-phenol. This was carbamoylated using general procedure 1 (CH2Cl2 was used as solvent) to give the title product after purification by preparative HPLC (Gilson) (35%, oil).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07279470B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-47bbc5c9258c42a59a954da5675c2c30
Quellennotizuspto-grants-2007_10