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Ninhydrin → 1,3-Indandione, 2-(3,5-dimethyl-p-hydroxyphenyl)-2-hydroxy-

HRID 527121
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반응식

HRID 527121 반응식
[CH:1]1[CH:6]=[C:5]2[C:7]([C:9]([OH:13])(O)[C:10](=[O:11])[C:4]2=[CH:3][CH:2]=1)=[O:8].[CH3:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([CH3:21])[C:16]=1[OH:22]>C(O)(=O)C>[OH:13][C:9]1([C:19]2[CH:18]=[C:17]([CH3:21])[C:16]([OH:22])=[C:15]([CH3:14])[CH:20]=2)[C:10](=[O:11])[C:4]2[C:5](=[CH:6][CH:1]=[CH:2][CH:3]=2)[C:7]1=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10236NinhydrinHCID 113352,6-Dimethylphenol

생성물 1

HCID 30544231,3-Indandione, 2-(3,5-dimethyl-p-hydroxyphenyl)-2-hydroxy-수율 20%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Ninhydrin (1.00 g, 5.61 mmol) and 2,6-dimethylphenol (686 mg, 5.61 mmol) was dissolved in acetic acid (15 ml), and this solution was heated for 13 hrs. The reaction mixture was concentrated, and extracted with dichloromethane, and then concentrated organic layer was purified using column chromatography (ethylacetate:hexane=1:2) to afford the title compound (0.31 g, 20%).

후처리

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  1. temperaturethis solution was heated for 13 hrs
  2. concentrationThe reaction mixture was concentrated
  3. extractionextracted with dichloromethane
  4. customconcentrated organic layer was purified

출처 및 근거

ORD 기록
ord-15ffb7cc92bb43df930f4f80ec36ab5f
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346749B2

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