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Toluene → HCID 9886503, 화합물

HRID 263974
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HRID 263974 반응식
[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[C:7]([Cl:11])=[CH:6][C:3]=1[CH:4]=O.[C:12]([CH2:15][C:16](=[O:18])[CH3:17])(=O)[CH3:13].Cl.[CH3:20][NH2:21].[C:22]1([CH3:28])C=CC=C[CH:23]=1.CCO[C:32]([CH3:34])=[O:33]>N1C=CC=CC=1>[C:16]([C:15]1[CH:4]([C:3]2[CH:6]=[C:7]([Cl:11])[C:8]([Cl:10])=[CH:9][C:2]=2[Cl:1])[C:23]([C:32](=[O:33])[CH3:34])=[C:22]([CH3:28])[N:21]([CH3:20])[C:12]=1[CH3:13])(=[O:18])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 1140TolueneHCID 8857Ethyl AcetateHCID 31261AcetylacetoneHCID 6101942,4,5-TrichlorobenzaldehydeHCID 6364545Methylamine hydrochloride

생성물 1

HCID 9886503HCID 9886503, 화합물수율 45%

시약·촉매·용매 1

HCID 1049
Pyridine
용매
2회

실험 절차

5.0 g (23.9 mmol) of 2,4,5-trichlorobenzaldehyde, 4.8 g (47.8 mmol) of acetylacetone and 1.78 g (26.3 mmol) of methylamine hydrochloride are boiled under reflux for 5 h in 4 ml of pyridine. The pyridine is then stripped off and the residue is codistilled twice with toluene. It is taken up in AcOEt and the solution is extracted with 1N aqueous HCl. Drying and concentration of the aqueous phase yields a brown oil, which is purified by flash chromatography (petroleum ether/AcOEt=5:1). The product is finally recrystallized from ether. 4.2 g of the title compound (45% of theory) are obtained. MS:385 Rf =0.65 (petroleum ether: AcOEt:=1:1)

후처리

  1. extractionthe solution is extracted with 1N aqueous HCl
  2. customDrying
  3. customconcentration of the aqueous phase yields a brown oil, which
  4. customis purified by flash chromatography (petroleum ether/AcOEt=5:1)
  5. customThe product is finally recrystallized from ether

출처 및 근거

ORD 기록
ord-0cfd4616a44744afb99f2c2b5fb03d06
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05646166

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