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Methanol → Methyl 4-(2-aminoethyl)benzoate

HRID 587923
ノート
印刷プレビュー

反応式

HRID 587923 の反応式
Cl.[NH2:2][CH2:3][CH2:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1.OS(O)(=O)=O.[CH3:19]O>>[NH2:2][CH2:3][CH2:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([O:11][CH3:19])=[O:10])=[CH:7][CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 162179904-(2-Aminoethyl)benzoic acid hydrochloride

生成物 1

HCID 11183521Methyl 4-(2-aminoethyl)benzoate

反応条件

温度
22 °C

実験手順

To a solution of 2.02 g (10.0 mmol) of 4-(2-aminoethyl)benzoic acid hydrochloride in 25 mL of methanol was added 1.5 mL of H2SO4. The mixture was heated to reflux and became a homogeneous solution after 1 h. The solution was refluxed for about 16 h, cooled to 22° C. and concentrated to about 10 mL by evaporation. The solution was diluted with 100 mL of water, made basic with 1 N NaOH and extracted with 100 mL of dichloromethane (DCM). The aqueous layer was back-extracted with DCM (4×100 mL). The combined extracts were dried (Na2SO4) and evaporated to give methyl 4-(2-aminoethyl)benzoate as a colorless oil. The material was used directly in the subsequent transformation.

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux
  3. customafter 1 h
  4. temperatureThe solution was refluxed for about 16 h
  5. concentrationconcentrated to about 10 mL by evaporation
  6. additionThe solution was diluted with 100 mL of water
  7. extractionextracted with 100 mL of dichloromethane (DCM)
  8. extractionThe aqueous layer was back-extracted with DCM (4×100 mL)
  9. dry with materialThe combined extracts were dried (Na2SO4)
  10. customevaporated

出典と根拠

ORDレコード
ord-ab2dff61208649459be34f0a6407ca45
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09227918B2

反応ノート

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