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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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Hydrochloric Acid → Hexafluoroacetone monohydrate

HRID 1818092
ノート
印刷プレビュー

反応式

HRID 1818092 の反応式
[F:1][C:2]([F:13])([F:12])[C:3]([C:8]([F:11])([F:10])[F:9])([OH:7])C([O-])=[O:5].[K+].Cl.C(=O)([O-])O.[K+].Cl[O-].[Na+]>>[OH2:5].[F:1][C:2]([F:13])([F:12])[C:3]([C:8]([F:11])([F:10])[F:9])=[O:7]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 516893Potassium BicarbonateHCID 23665760Sodium HypochloriteHCID 23683893Potassium 3,3,3-trifluoro-2-trifluoromethyl-2-hydroxypropionate

生成物 1

HCID 61525Hexafluoroacetone monohydrate

反応条件

温度
40 °C

実験手順

In a 100-ml three-necked flask was placed 6.52 g (14.8 mmol) of the 56.8% aqueous potassium 3,3,3-trifluoro-2-trifluoromethyl-2-hydroxypropionate solution prepared in Reference Example 1. To this mixture were added 1.7 g of 35% hydrochloric acid and 0.8 g of potassium hydrogencarbonate in this order, thereby adjusting the pH to 8. Subsequently, 24.0 g (32.3 mmol) of 10% aqueous sodium hypochlorite solution was added over one hour while heating the mixture at 40° C. in a water bath, followed by further stirring for 5 hours while maintaining the same temperature. The pH when the reaction was complete was 8. Hexafluoroacetone hydrate was obtained at a starting material conversion of 90% with a selectivity of at least 99%.

後処理

  1. customIn a 100-ml three-necked flask was placed
  2. temperaturewhile maintaining the same temperature

出典と根拠

ORDレコード
ord-6bb9f60611af4ea6b0fac75052244c90
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07598425B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート