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HRID 37298作成日:2026年10月26日

Cyclododecanemethanol → Cyclododecanecarboxaldehyde

https://huagongshe.com/reaction/37298

反応式

関与物質

役割名称HCID仕込み量
反応物CyclododecanemethanolHCID 74686—
反応物Sodium BromideHCID 253881—
反応物Sodium BicarbonateHCID 516892—
反応物TempoHCID 2724126—
反応物Sodium HypochloriteHCID 23665760—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物CyclododecanecarboxaldehydeHCID 7873796.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420153
出典データセットuspto-grants-1995_05
ORD IDord-38da7748ad104fcca20b5b9611834741
出典メモuspto-grants-1995_05