참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-(Benzyloxy)benzaldehyde | HCID 344784 | — |
| 반응물 | HCID 178503242 | HCID 178503242 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanol | HCID 67459728 | 95% |
반응 단계
In a nitrogen stream, a solution of 4-methylsulfanyl-phenylmagnesium bromide in THF (0.5 M, 35 mL) was added dropwise to a solution of 2-benzyloxybenzaldehyde (2.60 g, 12.2 mmol) in THF (24 mL) at 0° C. and the mixture was stirred at room temperature for two hours, and then a saturated ammonium chloride aqueous solution was added thereto under cooling with ice 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 (1:4)] to obtain the title compound (3.91 g, 95%).
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-e56e184b5ef54d4f90254602f3a895b4 |
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| 출처 메모 | uspto-grants-2011_11 |
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