Hydroxyamine hydrochloride → 4-Phenoxyphenoxyacetone oxime

HRID 35279노트

반응식

HRID 35279 반응식
Cl.[NH2:2][OH:3].C([O-])(=O)C.[Na+].[O:9]([C:16]1[CH:26]=[CH:25][C:19]([O:20][CH2:21][C:22](=O)[CH3:23])=[CH:18][CH:17]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>O.C(O)C>[O:9]([C:16]1[CH:26]=[CH:25][C:19]([O:20][CH2:21][C:22](=[N:2][OH:3])[CH3:23])=[CH:18][CH:17]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

참가 물질

6

실험 절차

Over about 1 hour, a solution of 22 g of hydroxylamine hydrochloride and 26 g of anhydrous sodium acetate in 110 ml of water is added dropwise at room temperature to a solution of 64 g of 4-phenoxyphenoxyacetone in 260 ml of ethanol. After the slightly exothermic reaction has subsided, the mixture is stirred for a further 3.5 hours at reflux temperature. Subsequently, the ethanol is distilled off from the reaction mixture by rotary evaporation, the aqueous residue is extracted three times with a 2:1 mixture of ether and hexane, the combined organic phases are washed with water and with 10% sodium bicarbonate solution and then dried over sodium sulfate. The solvent is then distilled off. Recrystallisation from a mixture of diethyl ether and pentane affords 4-phenoxyphenoxyacetone oxime with a melting point of 59°-61° C.

후처리

  1. customAfter the slightly exothermic reaction
  2. temperatureat reflux temperature
  3. distillationSubsequently, the ethanol is distilled off from the reaction mixture by rotary evaporation
  4. extractionthe aqueous residue is extracted three times
  5. additionwith a 2:1 mixture of ether and hexane
  6. washthe combined organic phases are washed with water and with 10% sodium bicarbonate solution
  7. dry with materialdried over sodium sulfate
  8. distillationThe solvent is then distilled off
  9. customRecrystallisation
  10. additionfrom a mixture of diethyl ether and pentane

출처 및 근거

ORD 기록
ord-f4cb6a7e299043e7b3155f8a624b2916
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04766152

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