Hydrochloric Acid → (R)-2-Methyl-2-trifluoromethoxymethyl-but-3-enoic acid
반응식
C[O:2][C:3](=[O:14])[C@@:4]([CH3:13])([CH2:7][O:8][C:9]([F:12])([F:11])[F:10])[CH:5]=[CH2:6].O.[OH-].[Li+].Cl>O1CCCC1.O>[CH3:13][C@:4]([CH2:7][O:8][C:9]([F:10])([F:12])[F:11])([CH:5]=[CH2:6])[C:3]([OH:14])=[O:2]참가 물질
반응 조건
- 온도
- 5 °C
실험 절차
A solution of crude (R)-2-methyl-2-trifluoromethoxymethyl-but-3-enoic acid methyl ester (98 mg) in tetrahydrofuran (4 mL) was stirred at 5° C. under nitrogen. A solution of lithium hydroxide monohydrate (63 mg, 1.5 mmol) in water (1 mL) was added and the reaction mixture was stirred at 5° C. for 1 h and then at room temperature for 3 days. Water was added and the mixture was acidified to pH 2 with hydrochloric acid (2 M) and the mixture was extracted with diethyl ether. The organic extracts were combined and washed with brine. The organic solution was filtered through a hydrophobic frit and the filtrate was evaporated to afford the crude title compound (95 mg) as a clear oil which was used in the next step. LCMS (m/z) 197.1 [M−H], Tr=2.16 min.
후처리
- waitat room temperature for 3 days
- extractionthe mixture was extracted with diethyl ether
- washwashed with brine
- filtrationThe organic solution was filtered through a hydrophobic frit
- customthe filtrate was evaporated
출처 및 근거
- ORD 기록
- ord-6cccb28b1e6845538c0ad7e1765485cb
- 출처 데이터셋
- uspto-grants-2015_06
- 특허 번호
- US09062092B2
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