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HRID 341988作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/341988

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 was 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US05856322
出典データセットuspto-grants-1999_01
ORD IDord-bf60d37ce04a456caee9f7ddf358b70b
出典メモuspto-grants-1999_01