関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Trichloro(chloromethyl)silane | HCID 15258 | — |
| 反応物 | HCID 178506676 | HCID 178506676 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | (Chloromethyl)(triphenyl)silane | HCID 261116 | — |
反応手順
A solution of 12.6 ml (18.4 g, 0.10 mol) of (chloromethyl)trichlorosilane in 150 ml of dry ether was stirred under nitrogen and chilled in ice while 162 ml (0.30 mol) of 1.85 molar phenyllithium in cyclohexane-ether 70:30 was added dropwise at a rate that held the mixture below 15° C. The resulting slurry was stirred overnight at room temperature, treated carefully with 10 ml of ethyl acetate to quench any remaining phenyllithium, washed with water and brine, dried over magnesium sulfate, and evaporated to leave 33 g of sticky solid. Recrystallization from 30 ml of cyclohexane provided 15.8 g (51%) of the title compound as an off white solid: m.p. 112°-115° C.; ir (Nujol®) 1420, 1110, 735, 730, 705, 695 cm-1 ; nmr (CDCl3) 3.5 (2H, s), 7.0-7.8 (15H, m).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04510136 |
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| 出典データセット | uspto-grants-1985_04 |
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| ORD ID | ord-4ebcbc91dd45421ab94367c53b75cbf1 |
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| 出典メモ | uspto-grants-1985_04 |
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