Diethyl Ether → HCID 21072857、化合物
反応式
C([C:4]1C=C(OC)[CH:7]=[CH:6][C:5]=1[NH:12][C:13](=[O:17])[O:14][CH2:15][CH3:16])(=O)C.[CH3:18][Mg]I.[Cl-].[NH4+].[CH2:23]([O:25][CH2:26][CH3:27])C>C1COCC1>[CH3:23][O:25][C:26]1[CH:27]=[CH:4][C:5]2[O:12][C:13](=[O:17])[NH:14][C:15]([CH3:16])([CH3:18])[C:6]=2[CH:7]=1参加物
実験手順
47.4 g (0.2 mol) of ethyl (2-acetyl-4-methoxyphenyl)carbamate, dissolved in 275 mL of THF, are added dropwise to a solution of 0.5 mol of methylmagnesium iodide in 200 mL of diethyl ether while cooling so that the temperature does not exceed 0° C. The mixture is stirred for 30 minutes at ambient temperature and then for 2 hours at reflux temperature. The reaction mixture is poured onto ice and combined with ammonium chloride. After the organic phase has been separated off, it is repeatedly extracted with ethyl acetate. The organic phases are combined, washed with water, dried with sodium sulfate, and evaporated down. The residue is dissolved in methanol and the solution is evaporated down and then combined with water. The precipitate formed is separated off, washed with water and recrystallized from toluene. Yield: 31.1 g (75%); m.p.=178° C.-180° C.
後処理
- temperaturewhile cooling so that the temperature
- customdoes not exceed 0° C
- temperaturefor 2 hours at reflux temperature
- additionThe reaction mixture is poured onto ice
- customAfter the organic phase has been separated off
- extractionit is repeatedly extracted with ethyl acetate
- washwashed with water
- dry with materialdried with sodium sulfate
- customevaporated down
- dissolutionThe residue is dissolved in methanol
- customthe solution is evaporated down
- customThe precipitate formed
- customis separated off
- washwashed with water
- customrecrystallized from toluene
出典と根拠
- ORDレコード
- ord-a604d9905aa141e9887da889cb93bc5e
- 出典データセット
- uspto-grants-2009_12
- 特許番号
- US07632834B2
反応ノート
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