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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 8-Methyl-8-azabicyclo(3.2.1)octan-3-ol | HCID 8424 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 8-Azabicyclo(3.2.1)octan-3-ol, 8-methyl-, 3-methanesulfonate | HCID 141951 | 78.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08207191B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-3f02659a912c4bbdaf5ea287d5bb31b1 |
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| 출처 메모 | uspto-grants-2012_06 |
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