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HRID 1785241作成日:2026年10月27日

Tributylphosphine → 3-{2-Methyl-4-[5-(4-trifluoromethyl-phenyl)-thiophen-2-ylmethoxy]-phenyl}-propionic acid methyl ester

https://huagongshe.com/reaction/1785241

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
反応物Methyl 3-(4-Hydroxy-2-methylphenyl)propanoateHCID 13551833—
反応物2-Thiophenemethanol, 5-[4-(trifluoromethyl)phenyl]-HCID 21986352—
溶媒TolueneHCID 1140—
溶媒HexaneHCID 8058—
生成物3-{2-Methyl-4-[5-(4-trifluoromethyl-phenyl)-thiophen-2-ylmethoxy]-phenyl}-propionic acid methyl esterHCID 68853010—

反応手順

To a solution of [5-(4-Trifluoromethyl-phenyl)-thiophen-2-yl]-methanol (0.063 g, 0.232 mmole) and 3-(4-Hydroxy-2-methyl-phenyl)-propionic acid methyl ester (0.045 g, 0.232 mmole) in toluene (2 mL) at room temperature, is added tributylphosphine (0.087 mL, 0.348 mmole) followed by a solution of 1,1′-(azodicarbonyl)-dipiperidine (0.088 g, 0.348 mmole) in toluene (2 mL). The reaction is stirred overnight, and then diluted with hexane (10 mL). The precipitate is removed through filtration and the filtrate is concentrated, loaded to a silica gel column, eluted with ethyl acetate in hexane (0-15%) and concentrated to provide the titled compound as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07504433B2
出典データセットuspto-grants-2009_03
ORD IDord-c3191e85e53f4984b08595ad3d44059a
出典メモuspto-grants-2009_03