Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129894Erstellt: 25. Oktober 2026

tert-Butanol → HCID 19370662, Verbindung

https://huagongshe.com/reaction/129894

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktSodium DithioniteHCID 24489—
EduktMethyl morpholine oxideHCID 82029—
Edukt1-(N-methylacetamido)-10-undeceneHCID 53922957—
KatalysatorOsmiumHCID 23937—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 19370662HCID 1937066270%

Reaktionsschritte

A solution of 1-(N-methylacetamido)-10-undecene (2.0 g, 8.9 mmol), N-methylmorpholine-N-oxide (4 mL of a 60% aqueous solution in water, 18 mmol) and potassium osmate dihydrate (10 mg) in acetone (50 mL), water (30 mL), and t-butanol (10 mL) was stirred at ambient temperature for 17 hours. Sodium dithionite (200 mg) was added to reduce the osmium catalyst. After 30 minutes, the mixture was added to dichloromethane (50 mL) and the layers separated. The aqueous layer was extracted with dichloromethane (3×50 mL). The combined organic layers were washed with saturated aqueous salt solution (50 mL) and dried over sodium sulfate, the solvent being subsequently evaporated under vacuum to a thick residue. The residue was purified by chromatography using silica and a dichloromethane/15% methanol eluant, resulting in 1.61 g of 1,2-dihydroxy-11-(N-methylacetamido)undecane (70% yield). This resulting diol (1.61 g, 6.2 mmol) was stirred in a 30% solution of hydrogen bromide in acetic acid (3.7 mL) for 1 hour. The solution was added to a mixture of sodium bicarbonate (7 g) in water (50 mL) and dichloromethane (25 mL). After bubbling ceased, the layers were separated and an aqueous layer extracted with dichloromethane (2×70 mL). The combined organic layers were washed with water (30 mL) and saturated aqueous salt solution (30 mL), then dried over sodium sulfate. The solvent was removed under vacuum to obtain 2.16 g of 1-(N-methylacetamido)-10-acetoxy-11-bromoundecane as a colorless oil (96% yield). Sodium methoxide (351 mg, 6.5 mmol) was added to a solution of bromoacetate (2.16 g, 5.9 mmol) in methanol (15 mL). After 1 hour of stirring, the mixture was added to water (25 mL) and extracted with dichloromethane (3×25 mL). The combined organic layers were washed with saturated aqueous salt solution (25 mL) and dried over sodium sulfate. The solvent was evaporated under vacuum and the residue purified with chromatography using silica and an ethyl acetate eluant, yielding 831 mg of 1,2-oxido-11-(N-methylacetamido)undecane (58% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05470878
Quelldatensatzuspto-grants-1995_11
ORD IDord-209502eda479439792966c505543c5bf
Quellennotizuspto-grants-1995_11