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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21427Erstellt: 25. Oktober 2026

Triethylamine → (R)-(+)-1,1,1-trifluoro-2-octyl 4-benzyloxybenzoate

https://huagongshe.com/reaction/21427

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-DimethylaminopyridineHCID 21885—
Edukt(R)-(+)-1,1,1-Trifluoro-2-octanolHCID 2779099—
Edukt4-BenzyloxybenzoylchlorideHCID 3766410—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-(+)-1,1,1-trifluoro-2-octyl 4-benzyloxybenzoateHCID 2285073061,2%

Reaktionsschritte

To a solution of 4-benzyloxybenzoic acid chloride (4.3 g) in methylene chloride (50 ml) was added a solution of (R)-(+)-1,1,1-trifluoro-2-octanol (2.9 g) ([α]D22.5 =+20.1, optical purity 96.3 % ee), dimethylaminopyridine (0.6 g) and triethylamine (1.7 g) in methylene chloride (50 ml) under ice-cooling. The mixture was left to stand at the room temperature for 24 hours before being poured in ice water. The methylene chloride layer separated was washed with diluted hydrochloric acid, water, 1N aqueous sodium carbonate solution and water in this order before being dried over magnesium sulfate. After distillation was over purification by toluene/silica gel chromatography and recrystallization from ethanol gave the titled compound (3.8 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424005
Quelldatensatzuspto-grants-1995_06
ORD IDord-85bfe5171bf14946843aa1a406d7b425
Quellennotizuspto-grants-1995_06