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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129894생성일: 2026년 10월 26일

tert-Butanol → HCID 19370662, 화합물

https://huagongshe.com/reaction/129894

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물Sodium DithioniteHCID 24489—
반응물Methyl morpholine oxideHCID 82029—
반응물1-(N-methylacetamido)-10-undeceneHCID 53922957—
촉매OsmiumHCID 23937—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물HCID 19370662HCID 1937066270%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05470878
출처 데이터셋uspto-grants-1995_11
ORD IDord-209502eda479439792966c505543c5bf
출처 메모uspto-grants-1995_11