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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1770062Erstellt: 26. Oktober 2026

Dicyclohexylcarbodiimide → (+)-4-[3-{2(S)-methylbutoxy}propyl]phenyl 4-decyloxybenzoate

https://huagongshe.com/reaction/1770062

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt4-PyrrolidinopyridineHCID 75567—
Edukt4-(Decyloxy)benzoic acidHCID 138527—
Edukt(+)-4-[3-{2(S)-methylbutoxy}propyl]phenolHCID 22844682—
Produkt(+)-4-[3-{2(S)-methylbutoxy}propyl]phenyl 4-decyloxybenzoateHCID 2284468390,4%

Reaktionsschritte

Into a four-necked flask equipped with a stirrer and a thermometer were charged 1.11 g (5 millimole) of (+)-4-[3-{2(S)-methylbutoxy}propyl]phenol, 1.67 g (6 millimole) of 4-decyloxybenzoic acid and 30 ml of anhydrous dichlomethane, and then 1.22 g (6 millimole) of N,N'-dicyclohexylcarbodiimide and 0.1 g of 4-pyrrolidinopyridine were added thereto, followed by stirring at room temperature for one day. After completion of the reaction, precipitates formed were filtered off and diluted with 200 ml of toluene. The organic phase was washed with water, 5% aqueous acetic acid solution, water, 5% aqueus sodium hydrogen carbonate solution and water in this order and then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromttography (eluent: toluene-ethyl acetate) to obtain 2.18 g (yield: 90.4%) of (+)-4-[3-{2(S)-methylbutoxy}propyl]phenyl 4-decyloxybenzoate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05385693
Quelldatensatzuspto-grants-1995_01
ORD IDord-b3b5a101e514463a82fb6d1fda8d861a
Quellennotizuspto-grants-1995_01