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Ammonium Chloride → 5-Benzyloxy 1-para-aminophenyl 1-pentanone

HRID 462720
ノート
印刷プレビュー

反応式

HRID 462720 の反応式
[CH2:1]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-])=O)=[CH:17][CH:16]=1)=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl-].[NH4+]>[Fe].C(O)C>[CH2:1]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([C:15]1[CH:16]=[CH:17][C:18]([NH2:21])=[CH:19][CH:20]=1)=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物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 132730465-Benzyloxy 1-para-nitrophenyl 1-pentanone

生成物 1

HCID 132730475-Benzyloxy 1-para-aminophenyl 1-pentanone

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 702Ethanol溶媒

実験手順

A mixture of 23 g of formula (IX) compound obtained in the preceding example and 23 g of powdered iron in 200 ml of an aqueous solution of 10% ammonium chloride and 20 ml of ethanol was left under agitation for an hour at room temperature. Then it was extracted with methylene chloride, filtered, the filtrate was washed with water, dried on sodium sulfate, filtered, the filtrate was evaporated and the residue crystallized in a mixture of ethyl acetate and isopropylic ether. 18.6 g of the expected compound were obtained.

後処理

  1. waitwas left under agitation for an hour at room temperature
  2. extractionThen it was extracted with methylene chloride
  3. filtrationfiltered
  4. washthe filtrate was washed with water
  5. customdried on sodium sulfate
  6. filtrationfiltered
  7. customthe filtrate was evaporated
  8. customthe residue crystallized in a mixture of ethyl acetate and isopropylic ether

出典と根拠

ORDレコード
ord-85922ff6c0a746a3b35fa11c48dc64ca
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04517197

反応ノート

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