참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Methyldiethoxysilane | HCID 74848 | — |
| 반응물 | 3-{4-[2-(2-Ethoxyethoxy)ethoxy]phenyl}-1-propene | HCID 20068004 | — |
| 촉매 | Chloroplatinic acid | HCID 61859 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | HCID 67933141 | HCID 67933141 | 97% |
반응 단계
This compound was made by first heating a mixture of 2.8 g (0.011 mol) of 3-{4-[2-(2-ethoxyethoxy)ethoxy]phenyl}-1 -propene (prepared as in Example 1), 5 g of benzene and 1.1 equivalent of methyldiethoxysilane under an argon atmosphere at 85° C. for one hour. After one hour, a trace amount (0.01 μL) of 1 part chloroplatinic acid in 1 part ethanol and 98 parts THF was added and the mixture was heated overnight at 85° C. The product was isolated by distillation to give 4.2 g (97%) of methyl diethoxy 3-{4-[2-(2-ethoxyethoxy)ethoxy]phenyl}propysilane, bp 135° C./0.08mm; NMR (δ): 0.20(3H,s), 0.65(2H,m), 1.05(9H,t), 1.50(2H,m), 2.70(2H,t), 3.90(12H,m), 7.0(2H,d), 7.15(2H,d).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04996277 |
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| 출처 데이터셋 | uspto-grants-1991_02 |
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| ORD ID | ord-f800b64e428b4683a36637fade35041f |
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| 출처 메모 | uspto-grants-1991_02 |
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