Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129526Erstellt: 24. Oktober 2026

Cyclododecanemethanol → Cyclododecanecarboxaldehyde

https://huagongshe.com/de/reaction/129526

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclododecanemethanolHCID 74686—
EduktSodium BromideHCID 253881—
EduktSodium BicarbonateHCID 516892—
EduktTempoHCID 2724126—
EduktSodium HypochloriteHCID 23665760—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktCyclododecanecarboxaldehydeHCID 7873796,1%

Reaktionsschritte

To a solution of 9.92 g (50 mmol) of cyclododecane methanol in 100 ml of methylene chloride under a nitrogen atmosphere is added 50 mg of 2,2,6,6-tetramethyl-1-piperidinyloxy, free radical (TEMPO) and 510 mg (5 mmol) of sodium bromide in 5 ml of water. The solution is cooled to 10°-15° C. and a solution of 100 ml of 5.25% aqueous sodium hypochlorite and 2.0 g of sodium bicarbonate is added over 1 hour. The reaction mixture is allowed to warm to room temperature and after 1 hour is diluted with methylene chloride. The organic phase is washed with aqueous sodium thiosulfate, aqueous bicarbonate and water. The methylene chloride layer is dried over magnesium sulfate, filtered and evaporated in vacuo to give 9.43 g of crude title compound as an oil: IR (film) 1723 cm-1 ; NMR (CDCl3)) δ 1.34 (bs, 18 H), 1.41 (m, 4 H), 1.54 (m, 2 H), 1.65 (m, 2 H), 2.40 (m, 1 H), 9.64 (d, 1 H, J=1.6 Hz) M+ (EI) 196

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468774
Quelldatensatzuspto-grants-1995_11
ORD IDord-5e4a7d55dcea4bc38d8a7c230fd2475e
Quellennotizuspto-grants-1995_11