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Cyclohexanone Oxime → Hydroxylammonium ammonium sulfate

HRID 437496
ノート
印刷プレビュー

反応式

HRID 437496 の反応式
[S:1](=[O:5])(=[O:4])([OH:3])[O-:2].[NH4+:6].C1(=[N:13][OH:14])CCCCC1.C1(=O)CCCCC1>>[OH:14][NH3+:13].[S:1]([O-:5])([O-:4])(=[O:3])=[O:2].[NH4+:6].[NH4+:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 7517Cyclohexanone OximeHCID 7967CyclohexanoneHCID 24655Ammonium bisulfate

生成物 1

HCID 86734871Hydroxylammonium ammonium sulfate

実験手順

The aqueous ammonium bisulfate phase freed from organic products such as cyclohexanone oxime and cyclohexanone may be used directly or, for example, after treatment with carbon for the removal of the final traces of organic components, in the catalytic hydroxylamine synthesis in place of sulfuric acid. Here again there is produced a hydroxylammonium/ammonium sulfate solution which may then be used for the oximation process. The aqueous ammonium bisulfate solution formed during oximation may, of course, be passed to the hydroxylamine synthesis as formed or, if desired, in a diluted or concentrated form. The oxime phase produced by the oximation reaction may be used directly, without post-oximation or purification, to particular advantage for catalytic rearrangement to caprolactam in the gas phase, the catalyst being, say, boron oxide/aluminum oxide.

後処理

  1. customafter treatment with carbon for the removal of the final traces of organic components
  2. customin the catalytic hydroxylamine synthesis in place of sulfuric acid

出典と根拠

ORDレコード
ord-f318fc406f294d00b4e4fa58ac873c36
出典データセット
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04031139

反応ノート

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