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2,4-Dichlorophenol → 2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran

HRID 905067
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인쇄 미리보기

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HRID 905067 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[OH:9].[H-].[Na+].S(O[CH2:23][CH:24]1[CH2:29][CH2:28][CH:27]=[CH:26][O:25]1)(C1C=CC(C)=CC=1)(=O)=O.C(=O)(O)[O-].[Na+]>CN(C)C=O>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[O:9][CH2:23][CH:24]1[CH2:29][CH2:28][CH:27]=[CH:26][O:25]1
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참가 물질

6

반응물 4

HCID 84492,4-DichlorophenolHCID 24758Sodium hydrideHCID 516892Sodium BicarbonateHCID 13071283(3,4-dihydro-2H-pyran-2-yl)methyl 4-methylbenzene-1-sulfonate

생성물 1

HCID 130712842-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran수율 76.1%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매
2회

실험 절차

A solution of 359 mg of 2,4-dichlorophenol in 3 ml of dimethylformamide was stirred with 96 mg of 55% sodium hydride at room temperature for 30 minutes. A solution of 536 mg of 2-tosyloxymethyl-3,4-dihydro-2H-pyran in 2 ml of dimethylformamide was then added, and the mixture was heated at 80°-90° C. for 2 hours. The reaction mixture was then cooled and poured onto a mixture of ice and sodium bicarbonate. The mixture was extracted with diethyl ether and the extract was dried over anhydrous potassium carbonate. After evaporation of the solvent, the residue was purified by column chromatography through silica gel eluted with a 1:2 by volume mixture of benzene and hexane, to give 394 mg of 2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran.

후처리

  1. temperaturethe mixture was heated at 80°-90° C. for 2 hours
  2. temperatureThe reaction mixture was then cooled
  3. extractionThe mixture was extracted with diethyl ether
  4. dry with materialthe extract was dried over anhydrous potassium carbonate
  5. customAfter evaporation of the solvent
  6. customthe residue was purified by column chromatography through silica gel
  7. washeluted with a 1:2 by volume mixture of benzene and hexane

출처 및 근거

ORD 기록
ord-b01f641e3ceb4fab9f08a7507462b0d4
출처 데이터셋
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04421758

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