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Formic Acid → 1,3-Benzodioxol-5-amine, N-methyl-

HRID 1266183
ノート
印刷プレビュー

反応式

HRID 1266183 の反応式
[CH2:1]1[O:10][C:9]2[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=2[O:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+].[CH:19](O)=O>O.CCOCC>[CH3:19][NH:6][C:5]1[CH:7]=[CH:8][C:9]2[O:10][CH2:1][O:2][C:3]=2[CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 284Formic AcidHCID 14798Sodium HydroxideHCID 843101,3-Benzodioxol-5-amineHCID 21226445Aluminium lithium hydride

生成物 1

HCID 106069191,3-Benzodioxol-5-amine, N-methyl-

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回
HCID 3283
Diethyl Ether
溶媒

実験手順

A solution of 3,4-methylenedioxyaniline (10 mmol) in formic acid (36 ml) is heated at reflux for 1 hour. After the removal of excess formic acid, the residue obtained is diluted with water and then extracted with dichloromethane. The combined organic phases are evaporated. The residue obtained is dissolved in ether, then lithium aluminium hydride (42 mmol) is added at 10° C., in small portions. After stirring the mixture at ambient temperature for 3 hours, water and 10% sodium hydroxide solution are added and the mixture is then filtered over Celite. The filtrate is dried and evaporated and the residue obtained is purified by chromatography on silica, using dichloromethane as eluant, to yield the expected product in the form of an oil.

後処理

  1. temperatureat reflux for 1 hour
  2. customAfter the removal of excess formic acid
  3. customthe residue obtained
  4. extractionextracted with dichloromethane
  5. customThe combined organic phases are evaporated
  6. customThe residue obtained
  7. filtrationthe mixture is then filtered over Celite
  8. customThe filtrate is dried
  9. customevaporated
  10. customthe residue obtained
  11. customis purified by chromatography on silica

出典と根拠

ORDレコード
ord-812a290eea024b6d9625f963c132b1f0
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06548515B1

反応ノート

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