참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzaldehyde | HCID 240 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Allyl bromide | HCID 7841 | — |
| 반응물 | HCID 178418365 | HCID 178418365 | — |
| 촉매 | HCID 178460666 | HCID 178460666 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 1-Phenylbut-3-en-1-ol | HCID 220119 | 94% |
반응 단계
To 0.30 ml (1.0 mmol) of tetraisopropoxytitanium and 5 ml of ethyl ether solution containing allyl bromide (1.0 mmol) was added dropwise at −50° C. 1.67 ml of 1.2M ethyl ether solution containing isopropylmagnesium bromide (2.0 mmol). Upon stirring at −50° C. to −40° C. for 1 hour, the reaction liquid turned from yellow into brown. To the reaction liquid was added 0.071 ml (0.7 mmol) of benzaldehyde at −45° C. to −40° C. The temperature was raised to −10° C. to 0° C. over 30 minutes. With 5 ml of 1N hydrochloric acid added, the solution was heated to room temperature and separated into layers. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate. After drying with anhydrous magnesium sulfate, the solution was freed of solvent by vacuum distillation. The residues were purified by silica gel chromatography. Thus there was obtained 97 mg of 1-phenyl-3-buten-1-ol (94% yields based on benzaldehyde).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06867161B1 |
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| 출처 데이터셋 | uspto-grants-2005_03 |
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| ORD ID | ord-da80cfd320f547a29825db22460bf3d6 |
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| 출처 메모 | uspto-grants-2005_03 |
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