反応式
[CH2:1]([OH:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10].C([O-])([O-])=O.[K+].[K+].[F:18][C:19]([P:25](Cl)[C:26]([F:32])([F:31])[C:27]([F:30])([F:29])[F:28])([F:24])[C:20]([F:23])([F:22])[F:21]>C(Cl)Cl>[F:24][C:19]([P:25]([C:26]([F:31])([F:32])[C:27]([F:28])([F:29])[F:30])[O:11][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10])([F:18])[C:20]([F:23])([F:22])[F:21]参加物
5
実験手順
0.31 g (1.9 mmol) of 9-decen-1-ol is initially introduced in CH2Cl2 with excess K2CO3, and 0.64 g (2.1 mmol) of bis(pentafluoroethyl)phosphinous acid chloride, (C2F5)2PCl, is condensed in. After the mixture has been stirred at room temperature for 30 minutes, the precipitate is filtered off, and volatile substances are removed in vacuo. The product, 9-decenyl bis(pentafluoroethyl)phosphinite, remains as a colourless, oily liquid, which is characterised by spectroscopy.
後処理
- customcondensed in
- filtrationthe precipitate is filtered off
- customvolatile substances are removed in vacuo
出典と根拠
- ORDレコード
- ord-c98278044eb643478b8fe43038cd321c
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08648202B2
関連ノート
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