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Sodium periodate → 2-Pyrrolidinone, 5-hydroxy-1-(phenylsulfonyl)-

HRID 1761888
ノート
印刷プレビュー

反応式

HRID 1761888 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 23667635Sodium periodate2 回HCID 178447417HCID 178447417、化合物

生成物 1

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

試薬・触媒・溶媒 3

HCID 30318Osmium Tetroxide触媒HCID 962Water溶媒HCID 312751,4-Dioxane
溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-218380039bd4432e9995d5892da13026
出典データセット
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04829079

反応ノート

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