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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247782Erstellt: 26. Oktober 2026

Chloride → Benzoic acid, 4-(phenylmethoxy)-, 1-(trifluoromethyl)nonyl ester

https://huagongshe.com/reaction/247782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorideHCID 312—
Edukt2-DimethylaminopyridineHCID 21885—
Edukt4-BenzyloxybenzoylchlorideHCID 3766410—
Edukt1,1,1-Trifluorodecan-2-olHCID 3864464—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
ProduktBenzoic acid, 4-(phenylmethoxy)-, 1-(trifluoromethyl)nonyl esterHCID 1474575396,3%

Reaktionsschritte

To a solution of 4-benzyloxybenzoic acid chloride (1.23 g) in methylene chloride (10 ml) was slowly added under ice cooling a solution of optically active 1,1,1-trifluoro-2-decanol (0.96 g), dimethylaminopyridine (0.55 g) and triethylamine (0.48 g) in methylane chloride (20 ml). The mixture was left to stand until it reached room temperature and allowed to react overnight. The mixture was poured in ice water and extracted with methylene chloride. The extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water in this order, and was dried over anhydrous magnesium sulfate. After the solution was distilled to remove the solvent, the crude product thus obtained was purified by toluene-silica-gel column chromatography and recrystallized from ethanol to obtain the titled compound (1.84 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05207947
Quelldatensatzuspto-grants-1993_05
ORD IDord-859e072770fa41648e889dcb531ae8cb
Quellennotizuspto-grants-1993_05