반응식
[K+].[Br-].CC1(C)N([O])C(C)(C)CCC1.[F:14][C:15]([F:27])([C:18]([F:26])([F:25])[C:19]([F:24])([F:23])[CH:20]([F:22])[F:21])[CH2:16][OH:17].[O-]Cl.[Na+].S(=O)(=O)(O)[OH:32]>CC#N.O>[F:14][C:15]([F:27])([C:18]([F:25])([F:26])[C:19]([F:23])([F:24])[CH:20]([F:21])[F:22])[C:16]([OH:32])=[O:17]참가 물질
실험 절차
5.2 ml water, 19 ml MeCN, 0.34 g KBr, TEMPO (0.12 g), and 6 g of 2,2,3,3,4,4,5,5-octafluoro-pentan-1-ol were placed in a 100 mL glass flask equipped with a dropping funnel and stirrer. 45 mL of 15% (wt) aq. NaOCl buffered to pH 8-9 were added via the dropping funnel in 3 portions over two days while stirring at room temperature. Then concentrated sulphuric acid were added to render the reaction mixture acidic. (pH 1-2). The reaction mixture was extracted three times with diethyl ether and the combined organic phases were dried over magnesium sulphate. The solvent was evaporated to give a colorless liquid (8.98 g), which was distilled using a water pump (15 mmHg, 73° C.) to give 5.13 g of the acid. Yield: 80%. 1H NMR (CDCl3): 6.08 (tt, J=52 Hz, J=5.3 Hz, 1H); 8.6 (s, 1H); 19F NMR (CDCl3): −120.6 (t, J=9.2 Hz, 2F); −125.81 (m, 2F); −130.61 (m, 2F); −138.4 (dm, J=52 Hz, 2F).
후처리
- customequipped with a dropping funnel and stirrer
- additionwere added via the dropping funnel in 3 portions over two days
- extractionThe reaction mixture was extracted three times with diethyl ether
- dry with materialthe combined organic phases were dried over magnesium sulphate
- customThe solvent was evaporated
출처 및 근거
- ORD 기록
- ord-b55ef902930d446496332faeba9a26a4
- 출처 데이터셋
- uspto-grants-2014_08
- 특허 번호
- US08809580B2
연결된 노트
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