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Acetic Acid → HCID 53812005, 화합물

HRID 990980
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HRID 990980 반응식
[O:1]=[C:2]1[C:10]2[C:5](=[CH:6][C:7]([NH:11][C:12](=[O:14])[CH3:13])=[CH:8][CH:9]=2)[CH2:4][CH2:3]1.[CH:15](=O)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C(O)(=O)C.N1CCCCC1>CO>[CH:15](=[C:3]1[CH2:4][C:5]2[C:10](=[CH:9][CH:8]=[C:7]([NH:11][C:12](=[O:14])[CH3:13])[CH:6]=2)[C:2]1=[O:1])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 240BenzaldehydeHCID 8082PiperidineHCID 312894N1-(1-oxo-2,3-dihydro-1H-inden-5-yl)acetamide

생성물 1

HCID 53812005HCID 53812005, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of N-(1-oxoindan-5-yl)acetamide (10.0 g, obtained from the Maybridge Chemical Co. Ltd), benzaldehyde (6.73 g), glacial acetic acid (1.06 g) and piperidine (10.8 g) was heated to 90° C. under nitrogen. Methanol (200 ml) was added and the mixture was cooled and then filtered to give N-(2-benzylidene-1-oxo-indan-5-yl)acetamide (13.47 g).

후처리

  1. customobtained from the Maybridge Chemical Co
  2. temperaturethe mixture was cooled
  3. filtrationfiltered

출처 및 근거

ORD 기록
ord-a7e9ee60c9f1473f8addba167aa7d804
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06462036B1

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