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Ethanol → Sodium 4-chloromethyl-7-hydroxy-8-methylcoumarin-4-methanesulfonate

HRID 1020925
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HRID 1020925 반응식
[Cl:1][CH2:2][C:3]1[C:12]2[C:7](=[C:8]([CH3:14])[C:9]([OH:13])=[CH:10][CH:11]=2)[O:6][C:5](=[O:15])[CH:4]=1.[S:16]([O-:19])([O-:18])=[O:17].[Na+:20].[Na+].[CH2:22](O)C>O>[Cl:1][CH2:2][C:3]1([CH2:22][S:16]([O-:19])(=[O:18])=[O:17])[C:12]2[C:7](=[C:8]([CH3:14])[C:9]([OH:13])=[CH:10][CH:11]=2)[O:6][C:5](=[O:15])[CH2:4]1.[Na+:20]
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참가 물질

5

반응물 3

HCID 702EthanolHCID 24437Sodium SulfiteHCID 54238774-(chloromethyl)-7-hydroxy-8-methyl-2H-chromen-2-one

생성물 1

HCID 86690062Sodium 4-chloromethyl-7-hydroxy-8-methylcoumarin-4-methanesulfonate수율 80%

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

A solution of 1 g of the compound 5 dissolved in 90 mL of ethanol is introduced into a flask, and then a solution of sodium sulfite (1.1 equivalents, 617 mg) in 22 mL of water is added. The mixture is refluxed. After 20 hours of heating, the mixture is cooled to 0° C. The solution is filtered on a Büchner funnel, the obtained beige residue is washed with ethanol, as for the filtrate, it is evaporated under reduced pressure in order to obtain a yellow solid. This solid is washed with ethanol and diethyl ether. Both obtained solids are collected in order to obtain 1 g (80%) of the crude compound 6.

후처리

  1. additionis introduced into a flask
  2. temperatureThe mixture is refluxed
  3. temperatureAfter 20 hours of heating
  4. filtrationThe solution is filtered on a Büchner funnel
  5. washthe obtained beige residue is washed with ethanol, as for the filtrate, it
  6. customis evaporated under reduced pressure in order
  7. customto obtain a yellow solid
  8. washThis solid is washed with ethanol and diethyl ether
  9. customBoth obtained solids are collected in order

출처 및 근거

ORD 기록
ord-907e5cf50bbc4ab8a37aa453eeef811d
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08716496B2

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