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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36137Erstellt: 24. Oktober 2026

p-Toluenesulfonic acid → 8-(3-Methylpentyloxy)octanol

https://huagongshe.com/de/reaction/36137

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktDimethylformamideHCID 6228—
Edukt3-Methyl-1-pentanolHCID 11508—
EduktSodium hydrideHCID 24758—
EduktHypobromous acidHCID 83547—
LösungsmittelMethanolHCID 887—
Produkt8-(3-Methylpentyloxy)octanolHCID 22407999—

Reaktionsschritte

To a solution of 1.67 gms of 3-methyl pentanol in 40 ml of dimethylformamide, 0.62 gms of sodium hydride are added; and the reaction mixture is stirred at room temperature for 1 hour. To this solution is added 4.0 gms of the protected bromo-alcohol and the reaction mixture is stirred at room temperature for 17 hours. The reaction mixture is then partitioned between ethyl acetate and water. The organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to give a yellow liquid. To a solution of 4.0 gms of this liquid in 240 ml of methanol is added 0.40 gms of p-toluenesulfonic acid and the reaction is stirred at room temperature for 16 hours. The methanol is removed under reduced pressure, and the residue is partitioned between ethyl acetate and water. The organic layer is washed with aqueous NaHCO3 and brine, then dried over Na2SO4, filtered, and concentrated under vacuum to give 8-(3-methylpentyloxy)octanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05412137
Quelldatensatzuspto-grants-1995_05
ORD IDord-4365ea31456546e198c66696939c2a4c
Quellennotizuspto-grants-1995_05