참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichlorodimethylsilane | HCID 6398 | — |
| 반응물 | Neophyl chloride | HCID 68191 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | HCID 178418740 | HCID 178418740 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Neophyldimethylchlorosilane | HCID 15495441 | 73% |
| 생성물 | HCID 178418740 | HCID 178418740 | — |
반응 단계
Neophylmagnesium chloride was prepared by the careful addition of 500 g (2.96 mol) of neophyl chloride to 75 g (3.125 mol) of magnesium turnings in 1.25 liters of dry THF. A five liter, 4-necked flask equipped with an overhead stirrer, condenser, thermometer and addition funnel was charged with 387 g (3.125 mol) of dimethyldichlorosilane, 3.0 g of cuprous cyanide and 250 ml of THF. Neophylmagnesium chloride was added dropwise from the addition funnel at such a rate as to maintain a gentle reflux. After the 2 hr. addition and additional 1 hr. reflux the reaction mixture was cooled, filtered and the filter cake was washed with hexane (2×250 ml). The combined organic layers were concentrated at reduced pressure and diluted with 100 ml hexane and again filtered. Reduced pressure concentration and distillation of the product gave 493 g (73% of theory) of neophyldimethylchlorosilane.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05296624 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-2f5ae81ddf22416b815e5848bef48eb0 |
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| 출처 메모 | uspto-grants-1994_03 |
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