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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37298Generated: October 25, 2026

Cyclododecanemethanol → Cyclododecanecarboxaldehyde

https://huagongshe.com/reaction/37298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclododecanemethanolHCID 74686—
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductCyclododecanecarboxaldehydeHCID 7873796.1%

Reaction Steps

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, 18H), 1.41 (m, 4H), 1.54 (m, 2H), 1.65 (m, 2H), 2.40 (m, 1H), 9.64 (d, 1H, J=1.6 Hz) M+ (EI) 196.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420153
Source datasetuspto-grants-1995_05
ORD IDord-38da7748ad104fcca20b5b9611834741
Source noteuspto-grants-1995_05