Triethylamine → N,N-diethyl-N'-(2,3-dihydro-6-methoxy-2-methyl-4-benzofuranyl)-1,2-ethanediamine dihydrochloride
反応式
[CH2:1]([N:3]([CH2:7][CH3:8])[CH2:4][CH2:5][Cl:6])[CH3:2].[K].[CH3:10][O:11][C:12]1[CH:13]=[C:14]2[O:18][CH:17]([CH3:19])[CH2:16][C:15]2=[C:20]([NH2:22])[CH:21]=1.C(N(CC)CC)C>C1(C)C=CC=CC=1>[ClH:6].[ClH:6].[CH2:1]([N:3]([CH2:7][CH3:8])[CH2:4][CH2:5][NH:22][C:20]1[C:15]2[CH2:16][CH:17]([CH3:19])[O:18][C:14]=2[CH:13]=[C:12]([O:11][CH3:10])[CH:21]=1)[CH3:2]参加物
6
実験手順
2.80 grams of 2-diethylamino-ethyl chloride and traces of potassium jodide are added to a solution of 3 grams of 2,3-dihydro-6-methoxy-2-methyl-4-benzofuranamine and 2.02 grams of triethylamine in 50 cc of anhydrous toluene and the resulting reaction mixture is refluxed for 16 hours. After cooling and washing with water, the toluene phase is dried over Na2SO4 and then concentrated to dryness. Hydrochloric acid is added to an ether solution of the resulting oily residue until a solid precipitates then the mixture is cooled. The precipitate is recovered on filter and recrystallized from ethanol by addition of ethyl ether, yielding 3.55 grams of the title compound. M.p. 158°-159° C.
後処理
- customthe resulting reaction mixture
- temperatureis refluxed for 16 hours
- temperatureAfter cooling
- washwashing with water
- dry with materialthe toluene phase is dried over Na2SO4
- concentrationconcentrated to dryness
- additionHydrochloric acid is added to an ether solution of the resulting oily residue until a solid
- customprecipitates
- temperaturethe mixture is cooled
- customThe precipitate is recovered
- filtrationon filter
- customrecrystallized from ethanol by addition of ethyl ether
出典と根拠
- ORDレコード
- ord-fc823c00d5df413ab68ff840184cb85a
- 出典データセット
- uspto-grants-1979_03
- 特許番号
- US04143055
反応ノート
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