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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 54184183, 화합물 → HCID 53931433, 화합물

HRID 261539
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HRID 261539 반응식
[CH3:1][O:2][C:3](=[O:19])[C:4](=O)[C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][C:13]=1[Cl:14])[CH2:10][C:9]([CH2:16][CH3:17])([CH3:15])[CH2:8]2.[H][H]>CO.S(=O)(=O)(O)O.[Pt](=O)=O>[CH3:1][O:2][C:3](=[O:19])[CH2:4][C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][C:13]=1[Cl:14])[CH2:10][C:9]([CH2:16][CH3:17])([CH3:15])[CH2:8]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 54184183HCID 54184183, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 53931433HCID 53931433, 화합물

시약·촉매·용매 3

HCID 345198Adams' catalyst촉매HCID 887Methanol용매HCID 1118Sulfuric Acid용매

실험 절차

A solution of 5.2 g of 2-ethyl-6-chloro-2-methyl-α-oxo-5-indanacetic acid methyl ester in 100 cc of methanol and 10 cc of concentrated sulphuric acid is hydrogenated at 45° and a hydrogen pressure of 5 atmospheres with the addition of 1.0 g of platinum(IV) oxide. After the take up of the theoretic amount of hydrogen the catalyst is filtered off, the solution is diluted with a 5% sodium bicarbonate solution and extracted with ether. The extract is washed with water, dried over sodium sulphate and concentrated by evaporation. The resulting title compound is purified by chromatography. Thin layer chromatogram: Rf value 0.60 (adsorbent: silica gel, eluant: chloroform).

후처리

  1. customis hydrogenated at 45°
  2. filtrationAfter the take up of the theoretic amount of hydrogen the catalyst is filtered off
  3. additionthe solution is diluted with a 5% sodium bicarbonate solution
  4. extractionextracted with ether
  5. washThe extract is washed with water
  6. dry with materialdried over sodium sulphate
  7. concentrationconcentrated by evaporation
  8. customThe resulting title compound is purified by chromatography

출처 및 근거

ORD 기록
ord-3c680a05fcd44f4d8351be645d3fcffd
출처 데이터셋
uspto-grants-1979_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04166131

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