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HRID 326908作成日:2026年10月26日

2-[(3-Bromophenyl)methoxy]oxane → 2-(3-Hydroxy-3-(3-((2-tetrahydropyranyloxy)methyl)phenyl)propyl)benzoic acid

https://huagongshe.com/reaction/326908

反応式

関与物質

役割名称HCID仕込み量
反応物2-[(3-Bromophenyl)methoxy]oxaneHCID 15282064—
反応物2-(3-Oxopropyl)benzoic acidHCID 53938421—
反応物HCID 178419628HCID 178419628—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3-Hydroxy-3-(3-((2-tetrahydropyranyloxy)methyl)phenyl)propyl)benzoic acidHCID 54411298—

反応手順

At -10° C., a solution of the aldehyde of Step 4 (5.045 g, 28.3 mmol) in 50 mL of THF was added dropwise to 0.57M 3-((2-tetrahydropyranyloxy)methyl)phenylmagnesium bromide in THF (120 mL, 68.4 mmol, prepared from the bromide of Step 2 and Mg in THF and filtered to remove the excess of Mg) and the mixture as stirred at r.t. for 30 min. At 0° C., 25% aq NH4OAc was added. The title product was extracted with EtOAc, dried over Na2SO4 and purified by flash chromatography on silica using acetone: toluene: HOAc 5:95:1 and 15:85:1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05270324
出典データセットuspto-grants-1993_12
ORD IDord-d8e33f1acad945bbb40926ab0ba800ae
出典メモuspto-grants-1993_12