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Ammonium Chloride → Ethyl 1-((2-amino-5-bromophenylamino)methyl)cyclopropanecarboxylate

HRID 1485428
ノート
印刷プレビュー

反応式

HRID 1485428 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N+:18]([O-])=O)=[C:6]([NH:8][CH2:9][C:10]2([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:12][CH2:11]2)[CH:7]=1.[Cl-].[NH4+]>[Fe].C(O)C>[NH2:18][C:5]1[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][C:6]=1[NH:8][CH2:9][C:10]1([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:11][CH2:12]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

5

反応物 2

HCID 25517Ammonium ChlorideHCID 70978279Ethyl 1-((5-bromo-2-nitrophenylamino)methyl)cyclopropanecarboxylate

生成物 1

HCID 86718502Ethyl 1-((2-amino-5-bromophenylamino)methyl)cyclopropanecarboxylate収率 76%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 702Ethanol溶媒

反応条件

温度
70 °C

実験手順

Iron powder (448 mg, 8.0 mmol) was added to a mixture of ethyl 1-((5-bromo-2-nitrophenylamino)methyl)cyclopropanecarboxylate (684 mg, 2.0 mmol), ammonium chloride aqueous (6 mL) and ethanol (20 mL). The reaction was heated to 70° C. and maintained at the 70° C. for 2 hours. The mixture solution was filtered. The filtrate was evaporated, diluted with water (100 mL), extracted with ethyl acetate (100 mL), and dried by sodium sulfate. The mixture was filtered. The filtrate was concentrated and purified by column chromatography (silica gel, petroleum ether/ethyl acetate=5:1) to give ethyl 1-((2-amino-5-bromophenylamino)methyl)cyclopropanecarboxylate (474 mg, 76%) as off-white solid.

後処理

  1. temperaturemaintained at the 70° C. for 2 hours
  2. filtrationThe mixture solution was filtered
  3. customThe filtrate was evaporated
  4. additiondiluted with water (100 mL)
  5. extractionextracted with ethyl acetate (100 mL)
  6. dry with materialdried by sodium sulfate
  7. filtrationThe mixture was filtered
  8. concentrationThe filtrate was concentrated
  9. custompurified by column chromatography (silica gel, petroleum ether/ethyl acetate=5:1)

出典と根拠

ORDレコード
ord-1dd255f9f9054a94a932c20a92f230d2
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09422292B2

反応ノート

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