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

HRID 462720
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HRID 462720 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 25517Ammonium ChlorideHCID 132730465-Benzyloxy 1-para-nitrophenyl 1-pentanone

생성물 1

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

시약·촉매·용매 2

HCID 23925Iron촉매HCID 702Ethanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-85922ff6c0a746a3b35fa11c48dc64ca
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04517197

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