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Pyridine → HCID 86735579, 화합물

HRID 1679691
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인쇄 미리보기

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HRID 1679691 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:9](=O)[CH2:10][CH2:11][CH2:12][CH2:13][O:14][CH3:15])[CH:5]=[CH:6][C:7]=1[Cl:8].Cl.Cl.[NH2:19][O:20][CH2:21][CH2:22][NH2:23].N1C=CC=CC=1>C(O)C>[ClH:1].[NH2:23][CH2:22][CH2:21][O:20][N:19]=[C:9]([C:4]1[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=1)[CH2:10][CH2:11][CH2:12][CH2:13][O:14][CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 143623262-(O-aminooxy)ethylamine dihydrochlorideHCID 584368751-(3,4-Dichlorophenyl)-5-methoxypentan-1-one

생성물 1

HCID 86735579HCID 86735579, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 14 mmol (3.65 g) of 3', 4'-dichloro-5-methoxyvalerophenone, 14 mmol (2.1 g) of 2-aminooxyethylamine dihydrochloride, 7 ml of pyridine and 14 ml of absolute ethanol was refluxed for 2 hours. The reaction mixture was then further processes as described in Example 4. After crystallization from a mixture of ether and petroleum ether (boiling point 40°-60° C) the above entitled compound was obtained with a melting point of 93°-94° C.

후처리

  1. temperaturewas refluxed for 2 hours
  2. customAfter crystallization
  3. additionfrom a mixture of ether and petroleum ether (boiling point 40°-60° C) the above entitled compound
  4. customwas obtained with a melting point of 93°-94° C.

출처 및 근거

ORD 기록
ord-26628989d15844feb9bf5cf70a328520
출처 데이터셋
uspto-grants-1978_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04081552

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