Borane;tetrahydrofuran → [2-(2-Chloro-4-nitrophenyl)ethyl]diethylamine

HRID 735122ノート

反応式

HRID 735122 の反応式
B.C1COCC1.[Cl:7][C:8]1[CH:13]=[C:12]([N+:14]([O-:16])=[O:15])[CH:11]=[CH:10][C:9]=1[CH2:17][C:18]([N:20]([CH2:23][CH3:24])[CH2:21][CH3:22])=O>C1COCC1>[Cl:7][C:8]1[CH:13]=[C:12]([N+:14]([O-:16])=[O:15])[CH:11]=[CH:10][C:9]=1[CH2:17][CH2:18][N:20]([CH2:21][CH3:22])[CH2:23][CH3:24]

参加物

4

実験手順

65 mL (65 mmol) of a 1M borane-THF solution is added dropwise to a solution of 3.7 g (13.67 mmol) of 2-(2-chloro-4-nitrophenyl)-N,N-diethylacetamide in 130 mL of THF at ambient temperature and stirred for 4 hours. Then the reaction mixture is evaporated down and the residue is combined with 15 mL of methanol and 15 mL of dilute hydrochloric acid. The mixture is then stirred for 15 minutes at 100° C., cooled, and diluted with water. Then the mixture is made alkaline with sodium carbonate solution and extracted twice with ethyl acetate. The combined organic phases are extracted twice with water and once with saturated saline solution and dried over sodium sulfate. The purification is carried out by column chromatography on Alox, neutral, act. II-III (eluant: petroleum ether/ethyl acetate (4:1)). Yield: 2.1 g (59.8% of theory); C12H17ClN2O2 (M=256.73); Rf value: 0.63 (Alox, petroleum ether/ethyl acetate (3:1)).

後処理

  1. customThen the reaction mixture is evaporated down
  2. stirringThe mixture is then stirred for 15 minutes at 100° C.
  3. temperaturecooled
  4. additiondiluted with water
  5. extractionextracted twice with ethyl acetate
  6. extractionThe combined organic phases are extracted twice with water and once with saturated saline solution
  7. dry with materialdried over sodium sulfate
  8. customThe purification

出典と根拠

ORDレコード
ord-f5d705e770c843f597c2aa4c71c8e792
出典データセット
uspto-grants-2009_09
特許番号
US07592373B2

反応ノート

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