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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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Isobutylene → 4-Penten-2-ol, 1,1,1-trifluoro-4-methyl-2-(trifluoromethyl)-

HRID 1021180
ノート
印刷プレビュー

反応式

HRID 1021180 の反応式
[F:1][C:2]([F:10])([F:9])[C:3]([C:5]([F:8])([F:7])[F:6])=[O:4].[CH3:11][C:12](=[CH2:14])[CH3:13].C(=O)=O.CC(O)C>>[F:1][C:2]([F:10])([F:9])[C:3]([C:5]([F:8])([F:7])[F:6])([OH:4])[CH2:13][C:12]([CH3:14])=[CH2:11]
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

4

反応物 3

HCID 8255Isobutylene2 回HCID 12695HexafluoroacetoneHCID 86586944Isopropanol carbon dioxide

生成物 1

HCID 124203304-Penten-2-ol, 1,1,1-trifluoro-4-methyl-2-(trifluoromethyl)-収率 83%

反応条件

温度
20 °C

実験手順

Hexafluoroacetone (238 g) and 120 g of isobutylene were condensed into a lecture bottle using Dry Ice/2-propanol cooling. The temperature was raised in the sealed vessel to 20° C. while stirring in a water bath and temperature maintained overnight. The next morning the temperature was raised to 50° C. for 2 hours. After cooling, excess isobutylene was bled off and the product distilled at 100-115° C. to afford 264 g (83%) of a clear liquid. The identity of the product was confirmed using 1H NMR spectroscopy and HRMS.

後処理

  1. customcondensed into a lecture bottle
  2. temperaturetemperature maintained overnight
  3. temperatureThe next morning the temperature was raised to 50° C. for 2 hours
  4. temperatureAfter cooling
  5. distillationthe product distilled at 100-115° C.

出典と根拠

ORDレコード
ord-55e0633404cb4f8d996d86f2af87c551
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08716535B2

反応ノート

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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