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Acetic Acid → HCID 54371093, 화합물

HRID 974779
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인쇄 미리보기

반응식

HRID 974779 반응식
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[CH2:5][CH2:6][C:7]2=[O:12].[S:13]1[CH:17]=[CH:16][CH:15]=[C:14]1[CH:18]=O.N1CCCCC1.C(O)(=O)C>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[CH2:5][C:6](=[CH:18][C:14]1[S:13][CH:17]=[CH:16][CH:15]=1)[C:7]2=[O:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 73642-ThiophenecarboxaldehydeHCID 8082PiperidineHCID 45474914-methoxy-2,3-dihydro-1H-inden-1-one

생성물 1

HCID 54371093HCID 54371093, 화합물수율 90%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
130 °C

실험 절차

To 4-methoxy-1-indanone (0.1 g; 0.62 mmol) were added thiophene-2-carboxaldehyde (87.5 μl ; 0.93 mmol), piperidine (18.5 μl ; 0.18 mmol) and acetic acid (10.7 μl ; 0.18 mmol). After heating at 130° C. for 90 minutes the mixture was taken up in CH2Cl2, washed with water and purified by flash chromatography, eluting with petroleum ether/ethyl acetate (95/5) to give 4-methoxy-2-(2-thienylmethylene)-1-indanone (140 mg; 90%).

후처리

  1. washwashed with water
  2. custompurified by flash chromatography
  3. washeluting with petroleum ether/ethyl acetate (95/5)

출처 및 근거

ORD 기록
ord-5d261c75f25f4b1a9cc61a7ea2abca42
출처 데이터셋
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05607928

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