Acetic Acid → HCID 23295939, compound

A mixture of N-(11,10-dihydroxyundecyl)piperidine (2.0 g, 7.4 mmol) and a 30% solution of hydrogen bromide in acetic acid (4.45 mL, 22 mmol) was stirred for 90 minutes. The mixture was then added to a flask containing aqueous sodium bicarbonate solution (15 g in 40 mL ) and dichloromethane (50 mL). After 10 minutes of vigorous stirring, the layers were separated and the aqueous portion extracted with dichloromethane (2×50 mL). The combined organic portions were dried over sodium sulfate. The solvent was evaporated to give 1-(10-acetoxy-11-bromoundecyl)piperidine which was used without further purification. Bromoacetate was dissolved in methanol (10 mL) and treated with a 1M solution of sodium methoxide (8 mL). After 30 minutes, the reaction mixture was added to water (30 mL) and extracted with dichloromethane (3×50 mL). The organic extracts were combined, washed with water (25 mL) and brine solution (25 mL) and then dried over anhydrous magnesium sulphate solution and concentrated under reduced pressure. The crude product obtained was further purified by column chromatography over alumina (grade-II) using 10% methanol/ethyl acetate eluant to yield 1.5 g (80.6%) N-(9,10-Oxidodecyl)piperidine.

1. additionThe mixture was then added to a flask
2. customthe layers were separated
3. extractionthe aqueous portion extracted with dichloromethane (2×50 mL)
4. dry with materialThe combined organic portions were dried over sodium sulfate
5. customThe solvent was evaporated

ORD record

ord-3584ef467cae49e48ee27376e9902ff3

Source dataset

uspto-grants-1999_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05866576