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Pyridine → 4-(4-t-Butylazo-4-cyanovaleryloxy)-2-hydroxybenzophenone

HRID 65891
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HRID 65891 반응식
[OH:1][C:2]1[CH:15]=[C:14]([OH:16])[CH:13]=[CH:12][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5].N1C=CC=CC=1.CCOCC.[C:28]([N:32]=[N:33][C:34]([C:41]#[N:42])([CH3:40])[CH2:35][CH2:36][C:37](Cl)=[O:38])([CH3:31])([CH3:30])[CH3:29]>O>[C:28]([N:32]=[N:33][C:34]([C:41]#[N:42])([CH3:40])[CH2:35][CH2:36][C:37]([O:16][C:14]1[CH:13]=[CH:12][C:3]([C:4]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)=[O:5])=[C:2]([OH:1])[CH:15]=1)=[O:38])([CH3:31])([CH3:29])[CH3:30]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1049PyridineHCID 3283Diethyl EtherHCID 85722,4-DihydroxybenzophenoneHCID 152740244-[(E)-tert-Butyldiazenyl]-4-cyanopentanoyl chloride

생성물 1

HCID 205634734-(4-t-Butylazo-4-cyanovaleryloxy)-2-hydroxybenzophenone수율 99%

시약·촉매·용매 1

HCID 962
Water
용매

실험 절차

To a solution of 4.7 g. (0.022 m) of 2,4-dihydroxybenzophenone and 2.5 ml. of pyridine in 35 ml. of ether in a 4 neck 100 ml. round bottom flask containing a thermometer, condenser and magnetic stirring bar was added 4.0 g. (0.0218 m) of 4-t-butylazo-4-cyanovaleryl chloride dropwise with cooling so the temperature did not rise above 25° C. After completion of the addition the reaction mixture was stirred 1/2 hour at room temperature and then diluted with 100 ml. of water. The ether layer was separated, washed consecutively with 5% HCl, water, and 10% NaHCO3 solution and saturated sodium chloride solution. The ether was evaporated off and the residue dissolved in methylene chloride, dried over anhydrous sodium sulfate, filtered and the methylene chloride stripped off under reduced pressure. The product weighted 8.8 g. (99% yield) and was a viscous syrup. The infrared spectrum was in agreement with the structure of the desired product.

후처리

  1. additionround bottom flask containing a thermometer, condenser and magnetic stirring bar
  2. additionwas added 4.0 g
  3. customdid not rise above 25° C
  4. additionAfter completion of the addition the reaction mixture
  5. additiondiluted with 100 ml
  6. customThe ether layer was separated
  7. washwashed consecutively with 5% HCl, water, and 10% NaHCO3 solution and saturated sodium chloride solution
  8. customThe ether was evaporated off
  9. dissolutionthe residue dissolved in methylene chloride
  10. dry with materialdried over anhydrous sodium sulfate
  11. filtrationfiltered

출처 및 근거

ORD 기록
ord-2c38ccc94d1546ba92a2bed4bc5bdd04
출처 데이터셋
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04129586

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