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Formaldehyde → Benzenemethanol,2-hydroxy-3,5-dimethyl-

HRID 371147
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HRID 371147 반응식
[CH2:1]=[O:2].[CH3:3][C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[CH:6][C:5]=1[OH:11].[OH-].[Na+]>O>[CH3:3][C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[C:6]([CH2:1][OH:2])[C:5]=1[OH:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 77712,4-DimethylphenolHCID 14798Sodium Hydroxide2회

생성물 1

HCID 11480550Benzenemethanol,2-hydroxy-3,5-dimethyl-

시약·촉매·용매 1

HCID 962Water용매

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온도
50 °C

실험 절차

A 38% solution of formaldehyde (32.0 grams, 0.4 mol) was added to a stirred solution of 2,4-dimethylphenol (36.6 grams, 0.3 mol) in water (100 ml) containing sodium hydroxide (14 gr., 0.35 mol) and heated at 50° C. for 4 to 5 hours. The reaction was cooled and solid sodium hydroxide added to precipitate the salt of the product. The solid was removed by filtration and dissolved in water. This solution was neutralized with carbon dioxide (dry ice) and the resulting mixture was extracted with methylene chloride. The organic layer was removed, dried, and evaporated to yield a light brown solid. This solid was washed in hexane containing a small amount of toluene to afford a tan solid. The NMR1 and FD/MS2 data support the structure.

후처리

  1. temperatureThe reaction was cooled
  2. customto precipitate the salt of the product
  3. customThe solid was removed by filtration
  4. dissolutiondissolved in water
  5. extractionthe resulting mixture was extracted with methylene chloride
  6. customThe organic layer was removed
  7. customdried
  8. customevaporated
  9. customto yield a light brown solid
  10. washThis solid was washed in hexane containing a small amount of toluene
  11. customto afford a tan solid

출처 및 근거

ORD 기록
ord-ee33765bf3bb4c019e4bcc67e00f7ef4
출처 데이터셋
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04529533

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