Hydrogen Bromide → HCID 54162042、化合物
反応式
[BrH:1].[F:2][CH:3]1[CH2:8][CH2:7][O:6][C:4]1=[O:5].[CH2:9](O)[CH3:10]>>[CH2:9]([O:6][C:4](=[O:5])[CH:3]([F:2])[CH2:8][CH2:7][Br:1])[CH3:10]参加物
4
実験手順
Hydrogen bromide gas was added over a period of about 30 minutes to a solution of 2-fluorobutyrolactone (1.8 g) in ethanol (15 ml) at 0° C. The reaction mixture was left at room temperature for 3 days, after which it was evaporated in vacuo. The residue was dissolved in icewater, the solution was neutralized with sodiumcarbonate and extracted with ether. The ether solution was washed with an aqueous saturated Na2SO4 solution, dried over Na2SO4 and evaporated to give 4-bromo-2-fluorobutyric acid ethyl ester (1.26 g, 34%). nD20 =1.4698. 1H-NMR (CDCl3, MeSi)δ: 1.3 (t, J=7 Hz, CH3); 2.1-2.8 (m, CH2); 3.55 (t, J=7 Hz, CH2Br); 4.3 (q, J=7 Hz, CH2); 4.75 and 5.55 (two triplets, J=6 Hz, CHF, JCHF =50 Hz).
後処理
- customafter which it was evaporated in vacuo
- dissolutionThe residue was dissolved in icewater
- extractionextracted with ether
- washThe ether solution was washed with an aqueous saturated Na2SO4 solution
- dry with materialdried over Na2SO4
- customevaporated
出典と根拠
- ORDレコード
- ord-44ae91d2a4b34399aa27dd4ba5215963
- 出典データセット
- uspto-grants-1985_01
- 特許番号
- US04495190
反応ノート
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