Trifluoroacetic acid → Methyl 2-{3-hydroxy-1-azabicyclo[2.2.2]octan-3-yl}acetate

Trifluoroacetic acid (40 mL) was added dropwise over 15 minutes to a solution of 2-(3-hydroxy-1-azabicyclo[2.2.2]oct-3-yl)acetic acid t-butyl ester (15.7 g) in anhydrous dichloromethane (40 mL) at 0° C. The mixture was stirred for 24 hours at room temperature, then the solvent was evaporated under reduced pressure. The residue was dissolved in methanol (90 mL) and cooled in an ice bath. Concentrated sulfuric acid (9 mL) was added dropwise over 10 minutes, then the reaction mixture was stirred at room temperature. After 3 hours, the solution was poured into 100 mL of ice water, basified to pH 10 with saturated aqueous sodium carbonate solution, and extracted with chloroform (4×100 mL). The extracts were dried (MgSO4), filtered, and evaporated in vacuo to give a solid. Recrystallization from ethyl acetate provided 6.3 g of the tan crystalline subtitle compound.

1. customthe solvent was evaporated under reduced pressure
2. dissolutionThe residue was dissolved in methanol (90 mL)
3. temperaturecooled in an ice bath
4. additionConcentrated sulfuric acid (9 mL) was added dropwise over 10 minutes
5. stirringthe reaction mixture was stirred at room temperature
6. waitAfter 3 hours
7. additionthe solution was poured into 100 mL of ice water
8. extractionextracted with chloroform (4×100 mL)
9. dry with materialThe extracts were dried (MgSO4)
10. filtrationfiltered
11. customevaporated in vacuo
12. customto give a solid
13. customRecrystallization from ethyl acetate

ORD 기록

ord-9ca5c103a2034145b1928055e9726dba

출처 데이터셋

uspto-grants-2004_03

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06706878B2