Triethylamine → N,N-diethyl-N'-(2,3-dihydro-6-methoxy-2-methyl-4-benzofuranyl)-1,2-ethanediamine dihydrochloride

HRID 614008ノート

反応式

HRID 614008 の反応式
[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

  1. customthe resulting reaction mixture
  2. temperatureis refluxed for 16 hours
  3. temperatureAfter cooling
  4. washwashing with water
  5. dry with materialthe toluene phase is dried over Na2SO4
  6. concentrationconcentrated to dryness
  7. additionHydrochloric acid is added to an ether solution of the resulting oily residue until a solid
  8. customprecipitates
  9. temperaturethe mixture is cooled
  10. customThe precipitate is recovered
  11. filtrationon filter
  12. 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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