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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium periodate → 2-Pyrrolidinone, 5-hydroxy-1-(phenylsulfonyl)-

HRID 1761888
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HRID 1761888 반응식
[C:1]1([S:7]([N-:10][C:11](=[O:16])[CH2:12][CH2:13][CH:14]=C)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.I([O-])(=O)(=O)=[O:18].[Na+]>O1CCOCC1.O.[Os](=O)(=O)(=O)=O>[C:1]1([S:7]([N:10]2[CH:11]([OH:16])[CH2:12][CH2:13][C:14]2=[O:18])(=[O:8])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 23667635Sodium periodate2회HCID 178447417HCID 178447417, 화합물

생성물 1

HCID 30867292-Pyrrolidinone, 5-hydroxy-1-(phenylsulfonyl)-수율 40.5%

시약·촉매·용매 3

HCID 30318Osmium Tetroxide촉매HCID 962Water용매HCID 312751,4-Dioxane
용매

실험 절차

50 mg of osmium tetraoxide is added to a solution of 5 g of N-benzenesulphonyl-4-pentenoylamide in 150 cm3 of dioxan and 50 cm3 of water. After about 20 minutes, 5.10 g of sodium metaperiodate is added, and after agitating for 1 hour, a further 5.10 g of sodium metaperiodate is added, with agitation for a further 2 hours at ambient temperature. The precipitate formed is filtered off, the filtrate is evaporated to dryness and the residue is dissolved in 50 cm3 of ethyl acetate, treated with activated charcoal, then evaporated to dryness. The residue is triturated in anhydrous ethyl ether, and 2.05 g of the expected product is obtained, which is re-crystallizxed from isopropanol m.p. 121° C.

후처리

  1. customThe precipitate formed
  2. filtrationis filtered off
  3. customthe filtrate is evaporated to dryness
  4. dissolutionthe residue is dissolved in 50 cm3 of ethyl acetate
  5. additiontreated with activated charcoal
  6. customevaporated to dryness
  7. customThe residue is triturated in anhydrous ethyl ether

출처 및 근거

ORD 기록
ord-218380039bd4432e9995d5892da13026
출처 데이터셋
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04829079

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