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Propylene Oxide → 2-Oxiranemethanesulfonyl azide

HRID 918357
ノート
印刷プレビュー

反応式

HRID 918357 の反応式
[CH2:1]([S:4]([N:7]=[N+:8]=[N-:9])(=[O:6])=[O:5])[CH:2]=[CH2:3].C([O-])(=[O:12])C.[Na+].C(OO)(=O)C.C=CC.O1C(C)C1>O.C(Cl)Cl.C(O)(=O)C>[O:12]1[CH2:3][CH:2]1[CH2:1][S:4]([N:7]=[N+:8]=[N-:9])(=[O:6])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 6378Propylene OxideHCID 6585Peracetic Acid2 回HCID 8252PropyleneHCID 517045Sodium AcetateHCID 20300589HCID 20300589、化合物

生成物 1

HCID 203005412-Oxiranemethanesulfonyl azide

試薬・触媒・溶媒 3

HCID 176
Acetic Acid
溶媒
HCID 962Water溶媒
HCID 6344Dichloromethane溶媒

実験手順

To a solution of 14.7 parts of 2-propene-1-sulfonyl azide in 105 parts of glacial acetic acid containing one part of sodium acetate was added with stirring at room temperature 40% peracetic acid in an amount in excess of that required to convert the propene radical to an epoxypropane radical. The reaction was stirred at room temperature until the peracetic acid content remained constant and then diluted with 200 parts of water and 135 parts of methylene chloride. The methylene chloride layer was removed and washed with water 5 times and then dried over magnesium sulfate. The methylene chloride solvent was removed leaving 15.1 parts of 2,3-epoxypropane-1-sulfonyl azide. The results of an infrared analysis of the product of % azido nitrogen and oxirane oxygen is tabulated below:

後処理

  1. customThe methylene chloride layer was removed
  2. washwashed with water 5 times
  3. dry with materialdried over magnesium sulfate
  4. customThe methylene chloride solvent was removed

出典と根拠

ORDレコード
ord-f375492158564d6fa358a602463784d1
出典データセット
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03971743

反応ノート

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