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4-Aminophenol → HCID 178500768, 화합물

HRID 255663
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HRID 255663 반응식
[CH:1]1[CH2:6][CH2:5][CH:4]([CH:7]=[CH:8][C:9](=[O:15])[CH2:10][C:11]([O:13][CH3:14])=[O:12])[CH2:3][CH:2]=1.[OH:16][C:17]1[CH:23]=[CH:22][C:20]([NH2:21])=[CH:19][CH:18]=1.[CH:24](OC(C)C)(C)C>C1C=CC=CC=1>[CH:1]1[CH2:6][CH2:5][CH:4]([CH:7]=[CH:8][C:9](=[O:15])[C:10](=[CH:24][NH:21][C:20]2[CH:22]=[CH:23][C:17]([OH:16])=[CH:18][CH:19]=2)[C:11]([O:13][CH3:14])=[O:12])[CH2:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 4034-AminophenolHCID 7914Diisopropyl EtherHCID 57308750Methyl 5-(cyclohexen-4-yl)-3-oxo-4-pentenoate

생성물 1

HCID 178500768HCID 178500768, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

In 20 ml benzene was dissolved 2.0 g of methyl 5-(cyclohexen-4-yl)-3-oxo-4-pentenoate, and 1.4 g of N,N-dimethylformamidodimethylacetal was added thereto. They were reacted at 70° C. for 1.5 hours. This reaction mixture was cooled to room temperature, and 1.2 g of p-hydroxyaniline was added thereto. They were reacted for 1.5 hours. After completion of the reaction, 50 ml of diisopropyl ether was added to the reaction mixture and the precipitated crystals were collected by filtration and washed with 20 ml of diisopropyl ether to obtain 2.1 g of methyl 5-(cyclohexen-4-yl)-2-(4-hydroxyphenylaminomethylene)-3-oxo-4-pentenoate having a melting point of 151°-153° C.

후처리

  1. additionwas added
  2. customThey were reacted at 70° C. for 1.5 hours
  3. customThey were reacted for 1.5 hours
  4. additionwas added to the reaction mixture
  5. filtrationthe precipitated crystals were collected by filtration
  6. washwashed with 20 ml of diisopropyl ether

출처 및 근거

ORD 기록
ord-590a37ab7b0b48cf87c8cc33676f7a85
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04698352

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