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Carbon tetrafluoride → Perfluoro 4,4-dimethyl-3-isopropyl-2-pentene

HRID 50411
ノート
印刷プレビュー

反応式

HRID 50411 の反応式
[F:1]C(F)(F)C(C(F)(F)F)=C(C(F)(F)C(F)(F)F)C(F)(C(F)(F)F)C(F)(F)F.FC([Si](C)(C)C)(F)F.[F-].[K+].FC(F)(F)F.[F:43][C:44]([F:75])([F:74])[C:45](C(F)(F)F)=[C:46]([C:60]([F:69])([C:65]([F:68])([F:67])[F:66])[C:61]([F:64])([F:63])[F:62])[C:47]([C:56]([F:59])([F:58])[F:57])([C:52]([F:55])([F:54])[F:53])[C:48]([F:51])([F:50])[F:49]>CN(C)C=O>[F:75][C:44]([F:43])([F:74])[C:45]([F:1])=[C:46]([C:60]([F:69])([C:61]([F:64])([F:62])[F:63])[C:65]([F:67])([F:68])[F:66])[C:47]([C:56]([F:59])([F:57])[F:58])([C:48]([F:51])([F:49])[F:50])[C:52]([F:53])([F:55])[F:54]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 6393Carbon tetrafluorideHCID 1216701,1,1,4,5,5,5-Heptafluoro-3-(pentafluoroethyl)-2,4-bis(trifluoromethyl)pent-2-eneHCID 522689Potassium Fluoride2 回HCID 552549(Trifluoromethyl)trimethylsilane2 回HCID 226420151,1,1,5,5,5-Hexafluoro-3-[1-(trifluoromethyl)-1,2,2,2-tetrafluoroethyl]-2,4,4-tris(trifluoromethyl)-2-pentene

生成物 1

HCID 73990785
Perfluoro 4,4-dimethyl-3-isopropyl-2-pentene

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

1 mmol (450 mg) of perfluoro(3-ethyl-2,4-dimethyl-2-pentene) and 4.0 mmol (568.8 mg) of trifluoromethyltrimethylsilane were weighed into a 10-ml fluororesin-made reaction container, then 1 ml of dimethyl formamide and 0.1 mmol of acidic potassium fluoride (KHF2, 7.8 mg) were added therein. A fluororesin-made magnetic stirrer was placed and the mixture was stirred vigorously for 1 hour at room temperature, and then 1.0 mmol of trifluoromethyltrimethylsilane (142.2 mg) and 0.1 mmol of acidic potassium fluoride (KHF2, 7.8 mg) were added and the mixture was further stirred vigorously for 1 hour at room temperature. After completion of the reaction, the transparent lower perfluorocarbon layer was analyzed by gas chromatography using a capillary column (NB-1, 0.25 μm, 1.5 mm ID×60 m). The yield of the main product perfluoro(2,4,4-trimethyl-3-isopropyl-2-pentene) was 74.5% by weight. As the by-product, perfluoro 4,4-dimethyl-3-isopropyl-2-pentene was obtained at the yield of 25.5% by weight. The starting material perfluoro(3-ethyl-2,4-dimethyl-2-pentene) was consumed completely by the reaction.

後処理

  1. customA fluororesin-made magnetic stirrer was placed
  2. stirringthe mixture was further stirred vigorously for 1 hour at room temperature
  3. customAfter completion of the reaction

出典と根拠

ORDレコード
ord-13ce255a86bf4c28b9543ff9474bc153
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06710214B2

反応ノート

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