反応式
[CH3:1][CH:2]1[CH2:7][CH2:6][O:5][C:4](=[O:8])[CH2:3]1.[CH2:9](O)[CH3:10].[BrH:12]>O>[CH2:9]([O:5][C:4](=[O:8])[CH2:3][CH:2]([CH3:1])[CH2:7][CH2:6][Br:12])[CH3:10]参加物
5
実験手順
A solution of 16.0 g. (0.14 mol) 4-methyl-3,4,5,6-tetrahydro-2-pyranone in 50 ml. anhydrous ethanol is saturated with hydrogen bromide gas at 0°-5° C., left to stand overnight, poured into water and extracted with diethyl ether. The combined ether extracts are dried over anhydrous sodium sulphate and evaporated and the residue is distilled in a vacuum to give 21.9 g. (70% of theory) of the desired product in the form of a colourless liquid; b.p. 85°-87° C./0.1 mm.; nD20 =1.4590.
後処理
- waitleft
- extractionextracted with diethyl ether
- dry with materialThe combined ether extracts are dried over anhydrous sodium sulphate
- customevaporated
- distillationthe residue is distilled in a vacuum
- customto give 21.9 g
出典と根拠
- ORDレコード
- ord-e193ada018fe4b62b03a9ff0bfef91c2
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04609673
関連ノート
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