참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isopropenyl acetate | HCID 7916 | — |
| 반응물 | Tri-o-tolylphosphine | HCID 80271 | — |
| 반응물 | Methoxytri-n-butylstannane | HCID 11964040 | — |
| 반응물 | 1-Bromo-3-((((1,1-dimethylethyl)dimethylsilyl)oxy)methyl)benzene | HCID 22033147 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Potassium Fluoride | HCID 522689 | — |
| 생성물 | 1-(3-((tert-Butyldimethylsilyloxy)methyl)phenyl)propan-2-one | HCID 57989269 | — |
반응 단계
A mixture of (3-bromobenzyloxy)(tert-butyl)dimethylsilane (16.72 g), isopropenyl acetate (9.2 mL), tri-n-butyltin methoxide (24 mL), palladium(II)acetate (0.625 g) and tri(o-tolyl)phosphine (1.70 g) in anhydrous toluene (65 mL) was heated at reflux at 100° C. for 5 hours and then left to cool overnight. The mixture was diluted with ethyl acetate (130 mL) and 4 molar aqueous potassium fluoride (80 mL) and stirred vigorously for 20 minutes. Diatomaceous earth was added and the suspension was then filtered through diatomaceous earth, washing the residue well with ethyl acetate. The combined filtrate and washings were dried over anhydrous magnesium sulphate and concentrated in vacuo and purified by flash chromatography on silica eluting with isohexane, 10% dichloromethane in isohexane and 20% diethyl ether in isohexane to afford the subtitled compound as a yellow oil. Yield 13.71 g.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08629271B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-902f7da4fb3e47b1af6d857ad950fbb6 |
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| 출처 메모 | uspto-grants-2014_01 |
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