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Acetic Acid → alpha-(2,4-Difluorophenyl)-n-[dimethyl(benzyloxymethyl)methyl]nitrone

HRID 636746
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HRID 636746 반응식
[F:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:3]=1[CH:4]=O.[CH3:11][C:12]([N+:23]([O-])=[O:24])([CH3:22])[CH2:13][O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C(O)(=O)C>C(O)C.[Zn]>[F:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[N+:23]([C:12]([CH3:22])([CH3:11])[CH2:13][O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[O-:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 176Acetic AcidHCID 737702,4-DifluorobenzaldehydeHCID 212556982-Methyl-2-nitro-1-benzyloxypropane

생성물 1

HCID 73197188alpha-(2,4-Difluorophenyl)-n-[dimethyl(benzyloxymethyl)methyl]nitrone수율 48%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 702
Ethanol
용매

실험 절차

A suspension of 2,4-difluorobenzaldehyde (443.7 mg, 3.12 mmol), 2-methyl-2-nitro-1-benzyloxypropane (639.4 mg, 3.06 mmol) and zinc (326.4 mg, 4.99 mmol) in ethanol (6 ml) was cooled to 0° C. in ice-water bath. Acetic acid (0.57 ml, 9.9 mmol) was added dropwise to the mixture. The mixture was gradually warmed to room temperature and stirred for 7 hours. The mixture was filtered through Celite® bed and the filtrate was concentrated and purified by silica gel chromatography (hexane/ethyl acetate=10/1-4/1) to give the title compound (468.8 mg; 48%).

후처리

  1. filtrationThe mixture was filtered through Celite® bed
  2. concentrationthe filtrate was concentrated
  3. custompurified by silica gel chromatography (hexane/ethyl acetate=10/1-4/1)

출처 및 근거

ORD 기록
ord-f375c44571e641538adcb015f072a831
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06194461B1

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