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Formaldehyde → 2,6-Dibenzyl-4-(hydroxymethyl)phenol

HRID 65292
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HRID 65292 반응식
[CH:1]([C:24]1[CH:29]=[C:28](CC2C=CC=CC=2)[C:27](O)=[C:26]([CH2:38][C:39]2[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=2)[CH:25]=1)([C:3]1[CH:8]=[C:7](CC2C=CC=CC=2)[C:6](O)=[C:5](CC2C=CC=CC=2)[CH:4]=1)C.[CH2:45]=[O:46].[OH-:47].[K+]>C(O)C>[CH2:38]([C:26]1[CH:27]=[C:28]([CH2:45][OH:46])[CH:29]=[C:24]([CH2:1][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)[C:25]=1[OH:47])[C:39]1[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 712Formaldehyde2회HCID 14797Potassium HydroxideHCID 20234424HCID 20234424, 화합물2회

생성물 1

HCID 137654732,6-Dibenzyl-4-(hydroxymethyl)phenol

시약·촉매·용매 1

HCID 702Ethanol용매3회

실험 절차

The desired alcohol was prepared by reaction of 2,6-dibenzylphenol with an equivalent of 37% aqueous solution of formaldehyde in ethanol. A solution of 6.85 grams of 2,6-dibenzylphenol in 5 mL ethanol was added to a solution of 1.65 grams 85% KOH in 5 mL ethanol and stirred for 30 minutes. About 1.91 mL of a 37% formalin solution was added dropwise at 25° C. and stirred overnight. The ethanol was removed from the purple solution by rotary evaporation and the residue was dissolved in methylene chloride, washed with saturated ammonium chloride solution and brine, and dried over sodium sulfate. Solvent removal provided 6.6 grams of a crude orange solid which was analyzed by gas chromatography as 4.1 grams starting material 2,6-dibenzylphenol and 2.2 grams 2,6-dibenzyl-4-hydroxymethylphenol (m.p. 116° C.).

후처리

  1. stirringstirred overnight
  2. customThe ethanol was removed from the purple solution by rotary evaporation
  3. dissolutionthe residue was dissolved in methylene chloride
  4. washwashed with saturated ammonium chloride solution and brine
  5. dry with materialdried over sodium sulfate
  6. customSolvent removal

출처 및 근거

ORD 기록
ord-46319aed988a4f1c9010db8af0f8d0f0
출처 데이터셋
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04613642

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