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HRID 554527作成日:2026年10月26日

Ammonium Chloride → (2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanol

https://huagongshe.com/reaction/554527

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2-(Benzyloxy)benzaldehydeHCID 344784—
反応物HCID 178503242HCID 178503242—
溶媒TetrahydrofuranHCID 8028—
生成物(2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanolHCID 6745972895%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08048897B2
出典データセットuspto-grants-2011_11
ORD IDord-e56e184b5ef54d4f90254602f3a895b4
出典メモuspto-grants-2011_11