참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4-(Methylthio)benzaldehyde | HCID 76985 | — |
| 반응물 | 1-(Benzyloxy)-2-bromobenzene | HCID 561828 | — |
| 반응물 | HCID 178418244 | HCID 178418244 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanol | HCID 67459728 | 58% |
반응 단계
In a nitrogen stream, an n-butyllithium hexane solution (1.59 M, 6.92 mL) was added dropwise to a solution of 1-benzyloxy-2-bromobenzene (2.89 g, 11.0 mmol) in THF (38 mL) at −78° C. and the mixture solution was stirred at the same temperature for 30 minutes. To this solution, a solution of 4-methylsulfanylbenzaldehyde (1.67 g, 11.0 mmol) in THF (12 mL) was added dropwise at −78° C. The reaction mixture was stirred at the same temperature for one hour, and then water was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:5)] to obtain the title compound (2.14 g, 58%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08048897B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-becdbd9e16964f3abdd2d43f65bd4051 |
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| 출처 메모 | uspto-grants-2011_11 |
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