Fluorotrimethylsilane → Tmsf ppve

HRID 275090

反応式

HRID 275090 の反応式
[C:1]([F:16])([O:5][C:6]([F:15])([F:14])[C:7]([F:13])([F:12])[C:8]([F:11])([F:10])[F:9])=[C:2]([F:4])[F:3].[Si:17]([F:21])([CH3:20])([CH3:19])[CH3:18].C(OC(C(F)(F)F)F)(C(C(F)(F)F)(F)F)(F)F>>[Si:17]([F:21])([CH3:20])([CH3:19])[CH3:18].[C:1]([F:16])([O:5][C:6]([F:14])([F:15])[C:7]([F:12])([F:13])[C:8]([F:9])([F:11])[F:10])=[C:2]([F:4])[F:3]

参加物

4

反応物 3

HCID 9869FluorotrimethylsilaneHCID 15388Perfluoro propyl vinyl etherHCID 94258Heptafluoropropyl 1,2,2,2-tetrafluoroethyl ether

生成物 1

HCID 131718260Tmsf ppve

実験手順

Example 8 was repeated using the same reactor and catalyst/support charge. CF3CF2CF2OCF(CF3)CO2SiMe3 (128.6 g, 0.320 mmol) was added dropwise at ca. 20 g/hr using N2 carrier flow of 34 mL/min. There was obtained 109.1 g of liquid product consisting of PPVE (49.4 mole %), TMSF (48.4%) and C3F7OCHFCF3 (2.2%). Distillation using a 24" spinning band column gave 23.9 g of an azeotrope (74/26 TMSF/PPVE by weight), 23.5 g of intermediate fractions, and 51.6 g of >99.8% purity PPVE.

後処理

  1. distillationDistillation

出典と根拠

ORDレコード
ord-f04e3a854d07493a96a880d634180466
出典データセット
uspto-grants-1995_02
特許番号
US05391796

関連ノート

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