참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Isobutyl chloride | HCID 10554 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | 3-Butyn-2-ol, 1,1,1-trifluoro-4-phenyl- | HCID 11412978 | — |
| 반응물 | HCID 178418368 | HCID 178418368 | — |
| 촉매 | Bis(cyclopentadienyl)titanium(IV) chloride | HCID 416358 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | HCID 20272630 | HCID 20272630 | 63% |
반응 단계
In an isobutylmagnesium chloride solution that was prepared by reacting isobutyl chloride (3.74 g, 40 mmol) and magnesium (0.97 g, 40 mmol) in dry ether (40 ml) at 0° C., dichlorobis(π-cyclopentadienyl)titanium (0.22 g, 0.9 mmol) and 1,1,1-trifluoro-4-phenyl-3-butyne-2-ol (2 g, 10 mmol) were slowly added at 0° C. After 4 hour agitation of the mixture at room temperature, solvent was removed under heating for 30 min. Next, dry tetrahydrofuran (20 ml) was put into the reaction vessel and further methyl iodide (12.7 g, 90 mmol) was slowly added. After 12 hour agitation, the reaction mixture was treated by a method similar to the one in the above Examples to obtain (Z)-1,1,1-trifluoro-4-phenyl-3-pentene-2-ol (b.p.: 84°-86° C./2 mmHg) at a yield of 63%. The above product gave the following analytical data:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04532020 |
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| 출처 데이터셋 | uspto-grants-1985_07 |
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| ORD ID | ord-c7b863e996644d2aa218b8222f6844f3 |
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| 출처 메모 | uspto-grants-1985_07 |
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