ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Formaldehyde → Propane, 2,2'-[methylenebis(oxy)]bis[1,1,1,3,3,3-hexafluoro-

HRID 2394988
ノート
印刷プレビュー

反応式

HRID 2394988 の反応式
S(=O)(=O)(O)O.[CH2:6]=[O:7].[CH:8]([OH:17])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10]>C(=O)=O.CC(C)=O>[CH:8]([O:17][CH2:6][O:7][CH:8]([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10]
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 712FormaldehydeHCID 1118Sulfuric AcidHCID 135291,1,1,3,3,3-Hexafluoro-2-propanol

生成物 1

HCID 9950185Propane, 2,2'-[methylenebis(oxy)]bis[1,1,1,3,3,3-hexafluoro-

試薬・触媒・溶媒 1

HCID 18522661Acetone cardice溶媒

実験手順

A 300 ml reactor, which had been cooled down in dry ice/acetone bath to -20° C., was charged with 111.3 g of fuming sulfuric acid, 9.3 g of paraformaldehyde and 52.8 g of HFIPA, followed by stirring for 20 minutes. After stopping stirring, it was cooled down to room temperature by standing still. With this, the contents were separated into two layers. The organic matter of the upper layer was taken out and then washed with 50 ml of 5% sodium hydrogencarbonate aqueous solution. With this, it was separated into two layers to obtain an organic matter.

後処理

  1. stirringAfter stopping stirring
  2. customWith this, the contents were separated into two layers
  3. washwashed with 50 ml of 5% sodium hydrogencarbonate aqueous solution
  4. customWith this, it was separated into two layers
  5. customto obtain an organic matter

出典と根拠

ORDレコード
ord-00e2ec1171864691aa16a1c2cff02e3c
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05811596

反応ノート

読み込み中…

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