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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Peroxide → HCID 178418378, 화합물

HRID 9517
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HRID 9517 반응식
O.[PH2:2]([O-:4])=[O:3].[Na+].[CH2:6]=[CH:7][CH2:8][CH2:9][CH2:10][CH3:11].OO>C(O)C.S(=O)(=O)(O)O>[CH2:6]([PH:2](=[O:4])[OH:3])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
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참가 물질

6

반응물 3

HCID 784Hydrogen Peroxide2회HCID 115971-HexeneHCID 178418950HCID 178418950, 화합물

생성물 1

HCID 178418378HCID 178418378, 화합물수율 82.4%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 1118Sulfuric Acid용매

실험 절차

To a mixture of 95.2 g (0.898 mol) of sodium hypophosphite hydrate in 600 mL 95% ethanol, 23.8 mL of concentrated sulfuric acid was added. 1-hexene (25.2 g, 0.30 mol) was added to the stirred mixture followed by 1.76 g (0.0155 mol) of 30% hydrogen peroxide. The resulting mixture was refluxed for 8 hs, and then another 1.14 g (0.0101 mol) of hydrogen peroxide was added and the reaction mixture was continued to reflux for another 8 hs. The resulting mixture was cooled, filtered, and then the ethanol was removed using a rotary evaporator. To the resulting residue, 200 mL water was added and then 50% sodium hydroxide solution was added until the solution became alkaline. The mixture was extracted twice with 200 mL diethyl ether, and the aqueous phase was then acidified with concentrated sulfuric acid. The aqueous layer was extracted with 200 mL ethyl acetate, and the organic layer was washed with saturated sodium chloride and then dried over anhydrous magnesium sulfate. The organic layer was decanted and the drying agent was washed with another 50 mL ethyl acetate. The combined organic layers were evaporated on a rotary evaporator. 37.0 g n-hexylphosphinic acid (82.4% yield) was obtained.

후처리

  1. additionwas added
  2. temperatureThe resulting mixture was refluxed for 8 hs
  3. temperatureto reflux for another 8 hs
  4. temperatureThe resulting mixture was cooled
  5. filtrationfiltered
  6. customthe ethanol was removed
  7. customa rotary evaporator
  8. additionTo the resulting residue, 200 mL water was added
  9. addition50% sodium hydroxide solution was added until the solution
  10. extractionThe mixture was extracted twice with 200 mL diethyl ether
  11. extractionThe aqueous layer was extracted with 200 mL ethyl acetate
  12. washthe organic layer was washed with saturated sodium chloride
  13. dry with materialdried over anhydrous magnesium sulfate
  14. customThe organic layer was decanted
  15. washthe drying agent was washed with another 50 mL ethyl acetate
  16. customThe combined organic layers were evaporated on a rotary evaporator

출처 및 근거

ORD 기록
ord-238025faf88247d8961dfc9c207d64dc
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07091262B2

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