참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Dimethoxydimethylsilane | HCID 66187 | — |
| 반응물 | HCID 178460902 | HCID 178460902 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | {3-(Triallylsilyl)propyl}(methoxy)dimethylsilane | HCID 86726597 | 72% |
반응 단계
Under a nitrogen atmosphere, dimethoxydimethylsilane (31) (1.0 ml, 7.0 mmol) was added to a reaction container, cooled down to 0° C., diethyl ether solution of 0.72M 3-(triallylsilyl)propylmagnesium bromide (24) (19.44 mL, 14 mmol) was added dropwise. After the dropwise adding, stirring was continued at room temperature for 5 hours. To the reaction mixture, water was added to stop the reaction, then 10% hydrochloric acid was added until the salt was completely dissolved. The obtained organic layer was separated and the obtained water layer was extracted with diethyl ether. The collected organic layer was washed each with saturated sodium bicarbonate aqueous solution and saturated saline solution in this order, dried over anhydrous magnesium sulfate, then filtered, concentrated under reduced pressure, obtaining {3-(triallylsilyl)propyl}(methoxy)dimethylsilane (32) represented by the following chemical reaction equation (yield: 1.5 g, yield (%): 72%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09228107B2 |
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| 출처 데이터셋 | uspto-grants-2016_01 |
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| ORD ID | ord-f1016c2e3f194fe49a9a49c06728a2d7 |
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| 출처 메모 | uspto-grants-2016_01 |
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