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HRID 459094作成日:2026年10月25日

4-Benzylphenol → (2S)-3-{4-[5-(4-Benzyl-phenoxy)-pent-1-ynyl]-phenyl}-2-methoxy-propionic acid

https://huagongshe.com/reaction/459094

反応式

関与物質

役割名称HCID仕込み量
反応物4-BenzylphenolHCID 7563—
反応物Cesium carbonateHCID 10796—
反応物3-[4-(5-Bromo-pent-1-ynyl)-phenyl]-2-methoxy-propionic acid ethyl esterHCID 69421973—
溶媒DimethylformamideHCID 6228—
生成物(2S)-3-{4-[5-(4-Benzyl-phenoxy)-pent-1-ynyl]-phenyl}-2-methoxy-propionic acidHCID 58822670—

反応手順

A solution of 3-[4-(5-Bromo-pent-1-ynyl)-phenyl]-2-methoxy-propionic acid ethyl ester from Step A (0.1 mmol, 1 eq) in 0.7 ml of DMF in a 16×100 mm tube treated with 4-hydroxydiphenylmethane (0.11 mmol, 1.1 eq) and Cesium Carbonate (0.3 mmol, 3 eq) and stirred at room temperature overnight. The reactants were filtered and washed with DMF several times. The solvent was evaporated under vacuo and the residue reconstituted in a mixture of Ethanol (2 ml) and NaOH (1M) (1 ml) and stirred at room temperature until reaction is completed by HPLC-MS. Then HCl (1M) was added (until pH=3) and the solvent were eliminated under vacuo. The residue was reconstituted in CH2Cl2/H2O and filtered through a hidrofobic syringer. The organic layer was separated, concentrated and purified by HPLC-MS to get the title compound. MS(ES) for C28H28O4[M+NH4]+: 446.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192982B2
出典データセットuspto-grants-2007_03
ORD IDord-c6e3361eb9e9459bb36ac4e54a7ea036
出典メモuspto-grants-2007_03