Lithium hydroxide, monohydrate → 4,4,4-Trifluoro-2-methylbutanoic acid
반응식
[F:1][C:2]([F:12])([F:11])[CH2:3][CH:4]([CH3:10])[C:5]([O:7]CC)=[O:6].O.[OH-].[Li+]>CO.O1CCCC1.O>[F:1][C:2]([F:12])([F:11])[CH2:3][CH:4]([CH3:10])[C:5]([OH:7])=[O:6]참가 물질
6
실험 절차
A solution of ethyl 4,4,4-trifluoro-2-methylbutyrate (7.7 g) in methanol (21 mL), tetrahydrofuran (21 mL) and water (8.4 mL) was treated with lithium hydroxide monohydrate (3.5 g). The mixture was stirred for 48 hours and the organic solvents evaporated. The resulting aqueous solution was diluted with water and acidified with 6N hydrochloric acid. The aqueous solution was exhaustively extracted with ethyl acetate. The combined organic extract was washed (water and brine), dried (MgSO4), filtered and evaporated to give 4,4,4-trifluoro-2-methylbutyric acid as a pale yellow liquid (6.5 g, 99%); partial NMR (300 MHz, CDCl3): 1.34 (d, 3H, CH3), 2.18 (m, 1H, H-C(3)), 2.67, (m, 1H, H-C(3)), 2.74 (m, 1H, H-C(2)), 10.6 (br, 1H, CO2H).
후처리
- customthe organic solvents evaporated
- additionThe resulting aqueous solution was diluted with water
- extractionThe aqueous solution was exhaustively extracted with ethyl acetate
- extractionThe combined organic extract
- washwas washed (water and brine)
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-8271f76a1228405ea9cc61edb2fdd05f
- 출처 데이터셋
- uspto-grants-1994_02
- 특허 번호
- US05286740
반응 노트
불러오는 중…