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Sodium Acetate → HCID 178449934, 화합물

HRID 2290676
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HRID 2290676 반응식
C([O-])(=O)C.[Na+].[Cl-].[CH2:7]([O:9][NH3+:10])[CH3:8].[C:11]([CH:16]1[C:21](=[O:22])[CH2:20][CH:19]([CH:23]2[CH:28]([CH3:29])[CH2:27][CH2:26][O:25][CH2:24]2)[CH2:18][C:17]1=[O:30])(=O)[CH2:12][CH2:13][CH3:14]>C(O)C>[CH2:7]([O:9][NH:10][C:11](=[C:16]1[C:17](=[O:30])[CH2:18][CH:19]([CH:23]2[CH:28]([CH3:29])[CH2:27][CH2:26][O:25][CH2:24]2)[CH2:20][C:21]1=[O:22])[CH2:12][CH2:13][CH3:14])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 517045Sodium AcetateHCID 19001768HCID 19001768, 화합물HCID 20229925HCID 20229925, 화합물

생성물 1

HCID 178449934HCID 178449934, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

3.69 parts by weight of sodium acetate and 3.51 parts by weight of ethoxyammonium chloride were added to 10.0 parts by weight of 2-butyryl-5-(4-methyltetrahydropyran-3-yl)-cyclohexane-1,3-dione in 100 ml of ethanol, and the mixture was stirred for 20 hours at room temperature. To work up the mixture, it was poured into ice water and extracted with methylene chloride, and the organic phase was washed with water, dried and evaporated down to give 10.7 parts by weight of 2-(1-ethoxyaminobutylidene)-5-(4-methyltetrahydropyran-3-yl)-cyclohexane-1,3-dione (active ingredient No. 1); nD22 =1.5235.

후처리

  1. extractionextracted with methylene chloride
  2. washthe organic phase was washed with water
  3. customdried
  4. customevaporated down

출처 및 근거

ORD 기록
ord-abb2670990a145c59f8ce5507f239216
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04618362

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