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Sodium Hydroxide → HCID 54035149, 화합물

HRID 1979688
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HRID 1979688 반응식
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([NH:15][C:16](=[O:21])[O:17][CH:18]([CH3:20])[CH3:19])[CH:7]=[C:8]([CH:13]=O)[C:9]=1[O:10][CH2:11][CH3:12])[CH3:2].[OH-].[Na+].Cl.[CH3:25][O:26][NH2:27]>C(O)C>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([NH:15][C:16](=[O:21])[O:17][CH:18]([CH3:20])[CH3:19])[CH:7]=[C:8]([CH:13]=[N:27][O:26][CH3:25])[C:9]=1[O:10][CH2:11][CH3:12])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 521874O-Methylhydroxylamine hydrochlorideHCID 13304036Propan-2-yl (3,4-diethoxy-5-formylphenyl)carbamate

생성물 1

HCID 54035149HCID 54035149, 화합물수율 93%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Isopropyl N-(3,4-diethoxy-5-formylphenyl)carbamate (0.6 g) was dissolved in ethanol (20 ml). To the solution was added an aqueous solution (10 ml) containing sodium hydroxide (0.32 g) and methoxyamine hydrochloride (0.66 g). After being allowed to stand for 12 hours, the reaction mixture was concentrated in vacuo, and the residue was dissolved in ethyl acetate. The resultant solution was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was washed with hexane to give isopropyl N-(3,4-diethoxy-5-methoxyiminomethylphenyl)carbamate (Compound No. 191) (0.61 g) in a yield of 93%. M.P., 110°-111.5° C.

후처리

  1. concentrationthe reaction mixture was concentrated in vacuo
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. washThe resultant solution was washed with water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. washThe residue was washed with hexane

출처 및 근거

ORD 기록
ord-afe94241f51642a1b166c749d861f73d
출처 데이터셋
uspto-grants-1984_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04482546

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