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Ethanol → 2-(4-Methyl-phenoxy)-5-methyl-phenylacetic acid

HRID 372420
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반응식

HRID 372420 반응식
[CH3:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][C:8]=2[CH2:14][C:15]#N)=[CH:4][CH:3]=1.C(O)C.[OH-:22].[K+].[OH2:24]>>[CH3:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][C:8]=2[CH2:14][C:15]([OH:24])=[O:22])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 702EthanolHCID 962WaterHCID 14797Potassium HydroxideHCID 543008532-(4-Methyl-phenoxy)-5-methyl-phenylacetonitrile

생성물 1

HCID 545247752-(4-Methyl-phenoxy)-5-methyl-phenylacetic acid

실험 절차

A solution of 95 g. of crude 2-(4-methyl-phenoxy)-5-methyl-phenylacetonitrile in 500 ml. of ethanol is treated with a solution of 67 g. of potassium hydroxide in 120 ml. of water and heated to reflux for 5 hours. Then, the ethanol is evaporated in vacuo and the residue diluted with 500 ml. of water. The resulting mixture is extracted twice with ether. The ethereal extracts are extracted twice with sodium bicarbonate solution. The combined aqueous solutions are acidified and extracted three times with ether. The ethereal extracts are washed with saturated sodium chloride solution, dried over sodium sulfate and evaporated in vacuo, and there is obtained 2-(4-methyl-phenoxy)-5-methyl-phenylacetic acid which, after recrystallization from methanol/water, melts at 101°-104° C.

후처리

  1. temperatureto reflux for 5 hours
  2. customThen, the ethanol is evaporated in vacuo
  3. additionthe residue diluted with 500 ml
  4. extractionThe resulting mixture is extracted twice with ether
  5. extractionThe ethereal extracts are extracted twice with sodium bicarbonate solution
  6. extractionextracted three times with ether
  7. washThe ethereal extracts are washed with saturated sodium chloride solution
  8. dry with materialdried over sodium sulfate
  9. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-e6337698f2254124a54e55a96f87aa7c
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04091023

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