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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 714240Erstellt: 25. Oktober 2026

Potassium Hydroxide → 3-(1-Phenylcyclohexyl)propanoic acid

https://huagongshe.com/reaction/714240

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktHydrazine hydrate (1:1)HCID 24654—
Edukt3-(2-Oxo-1-phenylcyclohexyl)propanoic acidHCID 200841—
LösungsmittelEthylene GlycolHCID 174—
Produkt3-(1-Phenylcyclohexyl)propanoic acidHCID 34398593%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

A mixture of 3-(2-oxo-1-phenylcyclohexyl)propanoic acid (1 g, 4.06 mmol), potassium hydroxide (0.770 g, 13.72 mmol), hydrazine monohydrate (0.348 mL, 6.09 mmol), and ethylene glycol (5 mL) was heated to 130° C. for 1.5 h. The condenser was removed and the mixture was heated to 200° C. for 30 min. The reaction mixture was then heated under reflux with a reflux condenser for additional 1.5 h. The reaction mixture was cooled to room temperature and diluted with 1N HCl to a total reaction volume of 25 mL. The precipitated product was collected by filtration, washed several times with water, and dried in vacuo to obtain 3-(1-phenylcyclohexyl) propanoic acid as a white solid (Int. 2, 923 mg, 93% yield). HPLC: tR=3.7 min, Chromolith SpeedRod 4.6×50 mm, 4 min gradient, Detection Wave length 220 nm, Starting solvent: 10% aq. MeOH-0.2% H3PO4; Final solvent: 90% aq. MeOH-0.2% H3PO4. LC/MS: m/e 215.19 (M+H-H2O)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187437B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-1776712fab244dc0955ec88584648612
Quellennotizuspto-grants-2015_11