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Acetic Acid → 8-Amino-6-methoxy-4-methyl-5-(5-phenylpentoxy)quinoline

HRID 1030183
ノート
印刷プレビュー

反応式

HRID 1030183 の反応式
[CH3:1][O:2][C:3]1[C:4]([O:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:5]2[C:10](=[C:11]([N+:13]([O-])=O)[CH:12]=1)[N:9]=[CH:8][CH:7]=[C:6]2[CH3:16].CC(O)=O.O(CCCC)CCCC>O.[Fe]>[NH2:13][C:11]1[CH:12]=[C:3]([O:2][CH3:1])[C:4]([O:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:5]2[C:10]=1[N:9]=[CH:8][CH:7]=[C:6]2[CH3:16]
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

6

反応物 3

HCID 176Acetic AcidHCID 8909Butyl etherHCID 198221476-Methoxy-4-methyl-5-(5-phenylpentoxy)-8-nitroquinoline

生成物 1

HCID 198221428-Amino-6-methoxy-4-methyl-5-(5-phenylpentoxy)quinoline収率 87%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 962Water
溶媒
2 回

反応条件

温度
80 °C

実験手順

A stirred mixture of 6-methoxy-4-methyl-5-(5-phenylpentoxy)-8-nitroquinoline (9.0 g, 0.024 mole), degreased 40 mesh Fe filings (22.5 g), H2O (90 ml), HOAc (18 ml) and Bu2O (18 ml) was heated at 80° C. for 1 h, cooled, diluted with H2O and filtered. The dark solid was thoroughly extracted with warm Et2O (total, Ca. 500 ml) and the extract was dried (Na2SO4), treated with charcoal and concentrated. The resulting dark brown oil was crystallized from pet ether to give 7.3 g (87%) of 8-Amino-6-methoxy-4-methyl-5-(5-phenylpentoxy)quinoline as yellow green crystals, mp 65°-66° C. This material was used without further purification.

後処理

  1. temperaturecooled
  2. filtrationfiltered
  3. extractionThe dark solid was thoroughly extracted with warm Et2O (total, Ca. 500 ml)
  4. dry with materialthe extract was dried (Na2SO4)
  5. additiontreated with charcoal
  6. concentrationconcentrated
  7. customThe resulting dark brown oil was crystallized from pet ether

出典と根拠

ORDレコード
ord-f911f577630c488695a1e83fdba13857
出典データセット
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05104885

反応ノート

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