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Malonic Acid → 3-Carboxy-6-methylcoumarin

HRID 276971
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인쇄 미리보기

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HRID 276971 반응식
[CH3:1][C:2]1[CH:9]=[C:6]([CH:7]=O)[C:5]([OH:10])=[CH:4][CH:3]=1.[C:11](O)(=[O:16])[CH2:12][C:13]([OH:15])=[O:14].N1C=CC=CC=1.NC1C=CC=CC=1>C(O)C.O>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:11](=[O:16])[C:12]([C:13]([OH:15])=[O:14])=[CH:7][C:6]=2[CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 867Malonic AcidHCID 1049PyridineHCID 6115AnilineHCID 69184Benzaldehyde, 2-hydroxy-5-methyl-

생성물 1

HCID 250903-Carboxy-6-methylcoumarin

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

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온도
40 °C

실험 절차

2 g of 5-methylsalicylaldehyde (14.7 mmol), 3.06 g of malonic acid (29.4 mmol), 1.3 g of pyridine and 0.08 g of aniline are dissolved in a minimum amount of ethanol. The mixture is heated at 40° C. on a water bath for 6 h. Next, it is diluted with water, acidified and then extracted with ether. The solvent is removed by distillation under reduced pressure. The residue obtained is recrystallized from ethanol.

후처리

  1. extractionextracted with ether
  2. customThe solvent is removed by distillation under reduced pressure
  3. customThe residue obtained
  4. customis recrystallized from ethanol

출처 및 근거

ORD 기록
ord-f1dfcf20fe7d423885f3648f9289de6e
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06355658B1

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