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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Peroxide → HCID 178449941, 화합물

HRID 1248777
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HRID 1248777 반응식
[Cl:1][CH:2]=[CH:3][CH2:4][O:5][N:6]=[C:7]([C@H:11]1[C:16](=[O:17])[CH2:15][C@H:14]([CH2:18][CH:19]([S:21][CH2:22][CH3:23])[CH3:20])[CH2:13][C:12]1=[O:24])[CH2:8][CH2:9][CH3:10].[OH:25]O>CC(C)=O>[Cl:1][CH:2]=[CH:3][CH2:4][O:5][N:6]=[C:7]([C@H:11]1[C:12](=[O:24])[CH2:13][C@H:14]([CH2:18][CH:19]([S:21]([CH2:22][CH3:23])=[O:25])[CH3:20])[CH2:15][C:16]1=[O:17])[CH2:8][CH2:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 178449940HCID 178449940, 화합물

생성물 1

HCID 178449941HCID 178449941, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

In this example, a mixture containing 2.2 g of trans-2-[1-(3-chloroallyloxyimino)butyl]-5-(2-ethylthiopropyl) cyclohexane 1,3-dione and 1 ml of aqueous 30% hydrogen peroxide in 10 ml of acetone was stirred at room temperature for about 21/2 days and then concentrated by evaporation. The residue was mixed with 50 ml of ethyl ether, washed with 30 ml of saturated aqueous sodium bicarbonate solution, then washed with 30 ml of water, dried over magnesium sulfate and evaporated to dryness affording 1.9 g of the title compound.

후처리

  1. concentrationconcentrated by evaporation
  2. additionThe residue was mixed with 50 ml of ethyl ether
  3. washwashed with 30 ml of saturated aqueous sodium bicarbonate solution
  4. washwashed with 30 ml of water
  5. dry with materialdried over magnesium sulfate
  6. customevaporated to dryness

출처 및 근거

ORD 기록
ord-ee6d8f7ca833453bb316d7c0fb4ab716
출처 데이터셋
uspto-grants-1986_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04626276

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