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Iodoethane → 4-(1-Ethyl-4-piperidinyl)-1-butanol

HRID 1044863
ノート
印刷プレビュー

反応式

HRID 1044863 の反応式
Cl.[NH:2]1[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][CH2:10][CH2:11][OH:12])[CH2:4][CH2:3]1.C(=O)([O-])[O-].[K+].[K+].I[CH2:20][CH3:21]>C(#N)C>[CH2:20]([N:2]1[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][CH2:10][CH2:11][OH:12])[CH2:4][CH2:3]1)[CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 27846674-(4-Piperidyl)-1-butanol hydrochloride

生成物 1

HCID 583060664-(1-Ethyl-4-piperidinyl)-1-butanol収率 55.9%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To stirring solution of 4-(4-piperidinyl)-1-butanol hydrochloride (4.51 g, 23.28 mmol) and potassium carbonate (8.04 g, 58.2 mmol) in dry acetonitrile (60 ml) was added iodoethane (2.070 ml, 25.6 mmol). The reaction mixture was allowed to stir at room temperature for 4 hours. The reaction mixture was concentrated in vacuo and the residue partitioned between water (20 ml) and ethyl acetate (30 ml). The aqueous was re-extracted with ethyl acetate (1×30 ml) then dichloromethane (1×30 ml), the organic layers dried by passage through a hydrophobic frit), combined and concentrated in vacuo to give the title compound as a yellow gum (2.41 g).

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customthe residue partitioned between water (20 ml) and ethyl acetate (30 ml)
  3. extractionThe aqueous was re-extracted with ethyl acetate (1×30 ml)
  4. dry with materialdichloromethane (1×30 ml), the organic layers dried by passage through a hydrophobic frit),
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-4dfcc2c2b8a44f54b4cde0af5f947f7c
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08563717B2

反応ノート

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