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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 554505생성일: 2026년 10월 25일

Water → (2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanol

https://huagongshe.com/reaction/554505

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-(Methylthio)benzaldehydeHCID 76985—
반응물1-(Benzyloxy)-2-bromobenzeneHCID 561828—
반응물HCID 178418244HCID 178418244—
용매TetrahydrofuranHCID 8028—
생성물(2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanolHCID 6745972858%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048897B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-becdbd9e16964f3abdd2d43f65bd4051
출처 메모uspto-grants-2011_11