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Water → Methyl (3-aminophenyl)carbamate

HRID 1033150
ノート
印刷プレビュー

反応式

HRID 1033150 の反応式
[Cl-].[NH4+].O.[CH3:4][O:5][C:6]([NH:8][C:9]1[CH:10]=[C:11]([N+:15]([O-])=O)[CH:12]=[CH:13][CH:14]=1)=[O:7]>[Fe].CC(O)C>[CH3:4][O:5][C:6]([NH:8][C:9]1[CH:10]=[C:11]([CH:12]=[CH:13][CH:14]=1)[NH2:15])=[O:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 4548185Methyl N-(3-nitrophenyl)carbamate

生成物 1

HCID 12877207Methyl (3-aminophenyl)carbamate収率 95.3%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 3776Isopropanol溶媒

実験手順

After refluxing a mixture of 37 g of iron powder, 1.9 g of ammonium chloride, 33 g of water, 13 g of 3-(methoxycarbonylamino)nitrobenzene, and 260 g of 2-propanol for 30 minutes, the reaction mixture was filtered under suction using sellaite. After extracting the product formed from the filtrate with ethyl acetate followed by washing with water, the product was dried by Glauber's salt. The solvent was distilled off from the product using an evaporator to provide 10.5 g (yield: 95%) of a black oily product.

後処理

  1. temperatureAfter refluxing
  2. filtrationthe reaction mixture was filtered under suction
  3. extractionAfter extracting the product
  4. customformed from the filtrate with ethyl acetate
  5. washby washing with water
  6. dry with materialthe product was dried by Glauber's salt
  7. distillationThe solvent was distilled off from the product
  8. customan evaporator

出典と根拠

ORDレコード
ord-559818628ca640d6b2a6ffe67d955ef0
出典データセット
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05310634

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート