참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methoxyphenol | HCID 9015 | — |
| 반응물 | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | HCID 178527255 | HCID 178527255 | — |
| 촉매 | Platinic chloride hexahydrate | HCID 134756 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
반응 단계
60.01 g of the intermediate siloxane of Formula 2, 83.43 g of hydroxyl polyethylene glycol allyl ether having an average molecular weight of about 750 (Uniox PKA5004, NOF Corporation), 120.00 g of 2-propanol (super dehydrated) (Wako Pure Chemical Industries), 0.60 g of 10% potassium acetate (Wako Pure Chemical Industries) in ethanol, 1.36 g of 1% 2,6-di-t-butyl-4-methylphenol (Wako Pure Chemical Industries) in 2-propanol and 0.69 g of 1% p-methoxyphenol (Wako Pure Chemical Industries) in 2-propanol were added into 500 ml eggplant-shaped flask. To this solution 1.20 g of 1% hydrogen hexachloroplatinate (IV) hexahydrate in 2-propanol (hereinafter 1% H2PtCl6/6H20/IPA) was added and stirred at 50° C. for 2 h. After that the reaction mixture was evaporated and vacuum-dried at 35° C. for 2 h. The reaction yielded 146.05 g of which about 80% was a hydrophilic polysiloxane, designated H10P16, having the structure of Formula 3 (above) wherein R2 is a methyl group, m is ˜20, n is ˜3, and p is ˜16. The polysiloxane had an HLB value of about 10 and a hydroxyl group content of about 1.2 wt. %. The remaining components of the reaction product were about 16% allyl PEG and about 4% PEG.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09322959B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-2f77afb51df44511a7b068689bcfa0f0 |
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| 출처 메모 | uspto-grants-2016_04 |
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