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Malonic Acid → 4-Hydroxy-7-methyl-benzo[h]chromen-2-one

HRID 1713711
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HRID 1713711 반응식
[CH3:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[OH:12].[C:13](O)(=[O:18])[CH2:14][C:15](O)=[O:16]>>[OH:18][C:13]1[C:6]2[C:7](=[C:8]3[CH:9]=[CH:10][CH:11]=[C:2]([CH3:1])[C:3]3=[CH:4][CH:5]=2)[O:12][C:15](=[O:16])[CH:14]=1
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참가 물질

3

반응물 2

HCID 867Malonic AcidHCID 113556405-Methylnaphthalen-1-ol

생성물 1

HCID 547180894-Hydroxy-7-methyl-benzo[h]chromen-2-one수율 43.3%

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온도
75 °C

실험 절차

The mixture of 5-methyl-1-naphthol (6) (1.0 g, 6.33 mmol), malonic acid (658 mg, 6.33 mmol), and PPA (10 g) was heated at 75° C. for 3 h. After the reaction, ice-water was added to the black residue. The solid was filtered, dissolved in 10% Na2CO3 solution, and stirred overnight. The basic solution was filtered, and the filtrate was acidified with 2 N HCl solution until the pH was about 4. The precipitate was then filtered and purified by silica gel chromatography to yield 7 (620 mg, 43%) as a yellow solid. mp 223-225° C.; 1H NMR (DMSO-d6) δ 2.69 (s, 3H), 5.70 (s, 1H), 7.57-7.61 (m, 2H), 7.86 (d, J=9.0 Hz, 1H), 7.92 (d, J=9.0 Hz, 1H), 8.23 (d, J=7.5 Hz, 1H), 12.8 (br s, 1H).

후처리

  1. additionwas added to the black residue
  2. filtrationThe solid was filtered
  3. dissolutiondissolved in 10% Na2CO3 solution
  4. filtrationThe basic solution was filtered
  5. filtrationThe precipitate was then filtered
  6. custompurified by silica gel chromatography

출처 및 근거

ORD 기록
ord-60eca7e07d5a457a9cabb69939a84fde
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07795299B2

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