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(2-Methoxymethoxyphenyl)(2-hydroxy-3-methoxyphenyl)methane → (2-Hydroxyphenyl)-(2-hydroxy-3-methoxyphenyl)methane

HRID 1111284
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HRID 1111284 반응식
COC[O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([O:18][CH3:19])[C:13]=1[OH:20]>CO.C1(C)C=CC(S(O)(=O)=O)=CC=1>[OH:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([O:18][CH3:19])[C:13]=1[OH:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 22151955(2-Methoxymethoxyphenyl)(2-hydroxy-3-methoxyphenyl)methane

생성물 1

HCID 22151938(2-Hydroxyphenyl)-(2-hydroxy-3-methoxyphenyl)methane

시약·촉매·용매 2

HCID 887Methanol용매HCID 6101p-Toluenesulfonic acid용매

실험 절차

(2-Methoxymethoxyphenyl)(2-hydroxy-3-methoxyphenyl)methane (3.95 g, 14 mmol) was dissolved in 150 ml of methanol containing 0.026 g of p-toluene sulfonic acid and the mixture was heated at reflux overnight. The volatiles were then removed by evaporation under reduced pressure and the solid that remained was taken up in ether. The ethereal solution was extracted with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated by evaporation under reduced pressure. The white solid residue was dried to obtain 3.66 g (99 percent of theory) of the title compound. The proton nmr spectrum was consistent with the assigned structure.

후처리

  1. temperaturethe mixture was heated
  2. temperatureat reflux overnight
  3. customThe volatiles were then removed by evaporation under reduced pressure
  4. extractionThe ethereal solution was extracted with saturated aqueous sodium bicarbonate
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated by evaporation under reduced pressure
  7. customThe white solid residue was dried

출처 및 근거

ORD 기록
ord-7cc9218b24b64759b0de983cd1e053d4
출처 데이터셋
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04979978

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