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Triethylamine → 4-(Methoxymethoxy)-3-methylbenzaldehyde oxime

HRID 393270
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인쇄 미리보기

반응식

HRID 393270 반응식
CCN(CC)CC.Cl.[NH2:9][OH:10].[CH3:11][O:12][CH2:13][O:14][C:15]1[CH:22]=[CH:21][C:18]([CH:19]=O)=[CH:17][C:16]=1[CH3:23]>O1CCOCC1.CCOC(C)=O>[CH3:11][O:12][CH2:13][O:14][C:15]1[CH:22]=[CH:21][C:18]([CH:19]=[N:9][OH:10])=[CH:17][C:16]=1[CH3:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 443297Hydroxyamine hydrochlorideHCID 226488754-(Methoxymethoxy)-3-methylbenzaldehyde

생성물 1

HCID 739911594-(Methoxymethoxy)-3-methylbenzaldehyde oxime수율 86.4%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane
용매

반응 조건

온도
25 °C

실험 절차

Et3N (1.68 mL, 12.0 mmol) and hydroxylamine hydrochloride (320 mg, 4.64 mmol) were added to a solution of 4-(methoxymethoxy)-3-methylbenzaldehyde (620 mg, 3.44 mmol) in 1,4-dioxane (12 mL). The reaction mixture was sonicated for 10 min and stirred at 25° C. for 3 d. The reaction mixture was diluted with EtOAc and successively washed with water and brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (Hexane:EtOAc, 3:1) to provide the title compound (580 mg, 86% yield) as a clear gum.

후처리

  1. customThe reaction mixture was sonicated for 10 min
  2. washsuccessively washed with water and brine
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by flash chromatography (Hexane:EtOAc, 3:1)

출처 및 근거

ORD 기록
ord-215eb0fea9fe401f9c785fc120fafbe8
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06806265B2

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