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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222142생성일: 2026년 10월 24일

8-Methyl-8-azabicyclo(3.2.1)octan-3-ol → 8-Azabicyclo(3.2.1)octan-3-ol, 8-methyl-, 3-methanesulfonate

https://huagongshe.com/ko/reaction/222142

반응식

참여 물질

역할이름HCID투입량
반응물8-Methyl-8-azabicyclo(3.2.1)octan-3-olHCID 8424—
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물Methanesulfonyl chlorideHCID 31297—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물8-Azabicyclo(3.2.1)octan-3-ol, 8-methyl-, 3-methanesulfonateHCID 14195178.1%

반응 조건

온도20 °C

반응 단계

Tropine (50 g) and triethylamine (60 mL, 43.56 g) in dichloromethane (1 L) were cooled to −10° C. Methane sulphonyl chloride (36 mL, 53.28 g) in dichloromethane (0.2 L) was added over 1 h at −5+/−2° C. After 0.5 h a solution of potassium carbonate (150 g) in water (0.4 L) was added and the mixture warmed to 20° C. The phases were separated and the aqueous phase extracted with further dichloromethane (1×0.2 L). The combined dichloromethane solution was concentrated by distillation collecting 1 L. n-Heptane (0.875 L) was added and the mixture stirred for 0.5 h. The solution was decanted off and then concentrated by distillation at 610 to 650 mbar until a solution temperature of 63° C. was reached. The solution was cooled to 0° C. with crystallization occurring during the cooling. The mixture was stirred for 1 h, the product isolated by filtration, washed and dried at <30° C. to give the title compound (60.62 g, 78.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207191B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-3f02659a912c4bbdaf5ea287d5bb31b1
출처 메모uspto-grants-2012_06