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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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3,3-Dimethoxybutan-2-ol → 3,3-Dimethoxy-2-butanone

HRID 1066557
ノート
印刷プレビュー

反応式

HRID 1066557 の反応式
[CH3:1][O:2][C:3]([O:8][CH3:9])([CH3:7])[CH:4]([OH:6])[CH3:5]>CC(=O)CC>[CH3:1][O:2][C:3]([O:8][CH3:9])([CH3:7])[C:4](=[O:6])[CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 1027943,3-Dimethoxybutan-2-ol

生成物 1

HCID 1408713,3-Dimethoxy-2-butanone

試薬・触媒・溶媒 1

HCID 6569Methyl Ethyl Ketone溶媒

実験手順

Advantageous starting materials of the formula II are also compounds in which X is 2 alkoxy groups. These can be obtained very advantageously, even industrially, by the electrochemical process described in EP 460 451 B1. Thus, for example, 3,3-dimethoxy-2-butanol, which is particularly suitable for the preparation of diacetyl, is obtained by this process from 2-butanone (methyl ethyl ketone) in a selectivity of 70% of theory (cf. Example 1A). From this, the novel process can be used to obtain 3,3-dimethoxy-2-butanone in yields above 90% (cf. Example 1B), which can be converted into diacetyl by alkaline or, preferably, acidic hydrolysis in a manner known per se in virtually quantitative yield. This is therefore a very advantageous overall process for the preparation of diacetyl from the readily available methyl ethyl ketone.

後処理

  • customThese can be obtained very advantageously
  • 出典と根拠

    ORDレコード
    ord-b94cf2ecc9b6471993fa309dd09d66f8
    出典データセット
    uspto-grants-2001_06
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06242653B1

    反応ノート

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