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Diethyl Ether → HCID 178486115、化合物

HRID 1578997
ノート
印刷プレビュー

反応式

HRID 1578997 の反応式
[Cl-].[CH3:2][N:3]([S+:5]([N:9]([CH3:11])[CH3:10])[N:6]([CH3:8])[CH3:7])[CH3:4].[O-:12][C:13]#[N:14].[Na+].CCOCC>CO>[O-:12][C:13]#[N:14].[CH3:2][N:3]([S+:5]([N:9]([CH3:11])[CH3:10])[N:6]([CH3:8])[CH3:7])[CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3283Diethyl EtherHCID 517096Sodium CyanateHCID 86733077HCID 86733077、化合物

生成物 1

HCID 178486115HCID 178486115、化合物収率 90%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of 10 g (0.05 mole) of tris(dimethylamino)sulfonium chloride and 3.6 g (0.055 mole) powdered sodium cyanate in 100 ml methanol was stirred at room temperature (25°) for 3 days. Ether, 300 ml, was added, and the precipitated sodium chloride was filtered off. The filtrate was evaporated to dryness under reduced pressure and the residue was redissolved in acetonitrile, filtered, and then precipitated by the addition of ether. The precipitate was collected on a filter, washed with ether, and dried under dry nitrogen to give 9.27 g (90%) of tris(dimethylamino)sulfonium cyanate as a white crystalline powder, m.p. 202°-204°.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationthe precipitated sodium chloride was filtered off
  2. customThe filtrate was evaporated to dryness under reduced pressure
  3. dissolutionthe residue was redissolved in acetonitrile
  4. filtrationfiltered
  5. customprecipitated by the addition of ether
  6. customThe precipitate was collected on a filter
  7. washwashed with ether
  8. customdried under dry nitrogen

出典と根拠

ORDレコード
ord-7cee66f468644d9985726c8e44ebeb95
出典データセット
uspto-grants-1976_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03940402

反応ノート

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