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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1421371Erstellt: 25. Oktober 2026

Methylparaben → 4-(2-Piperidinoethoxy)benzoic acid hydrochloride

https://huagongshe.com/reaction/1421371

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylparabenHCID 7456—
EduktPotassium CarbonateHCID 11430—
Edukt2,2,2-Trifluoroethanesulfonyl chlorideHCID 74242—
Edukt1-(Piperidin-1-yl)ethanolHCID 3030541—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelAmyl AcetateHCID 12348—
Produkt4-(2-Piperidinoethoxy)benzoic acid hydrochlorideHCID 574383593,2%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

Into a 50 ml round bottom flask is placed 4.93 g (27.0 mmol) of 2,2,2-trifluoroethanesulfonyl chloride and 25 ml of methylene chloride. The resulting solution is cooled with an ice bath as 3.22 g (24.9 mmol) of 1-piperidinoethanol in 7 ml of methylene chloride is added dropwise. After the addition is complete, the ice bath is removed and the resulting slurry is stirred for about 12 hours. The reaction mixture is concentrated on a rotary evaporator to yield a waxy residue. The solid residue is slurried in 45 ml of amyl acetate and then potassium carbonate (5.50 g, 39.9 mmol) and methyl 4-hydroxybenzoate (2.26 g, 14.8 mmol) are added. The resulting mixture is heated to 140° C. for 2 hours. The reaction mixture is cooled to room temperature and washed twice with water and the organic layer is extracted with 10.5 ml of 8 N hydrochloric acid. The aqueous layer is heated at gentle reflux for 4 hours. The resulting slurry is cooled to 50° C. and 11 ml of acetone is added. The slurry is cooled to 0-5° C. and stirred for 1 hour. The product is filtered, washed with cold acetone, and dried at 50° C. in vacuo to yield 3.94 g of product, (90%). 1H NMR. HPLC 96.9%. TRS 2.78%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06075146
Quelldatensatzuspto-grants-2000_06
ORD IDord-a468fc0052b347668176a6bfc4de27e6
Quellennotizuspto-grants-2000_06