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HRID 15005作成日:2026年10月24日

Methyl Acrylate → (E)-3-(3-Hydroxymethyl-phenyl)-acrylic acid methyl ester

https://huagongshe.com/ja/reaction/15005

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl AcrylateHCID 7294—
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物3-Iodobenzyl alcoholHCID 42300—
触媒palladium(II) acetateHCID 167845—
溶媒AcetonitrileHCID 6342—
生成物(E)-3-(3-Hydroxymethyl-phenyl)-acrylic acid methyl esterHCID 5979468897%

反応条件

温度100 °C

反応手順

The procedure described in Reich, S. H. etal. J. Med. Chem. 2000, 43, 1670 was followed. Pd(OAc)2 (8.2 mg, 0.037 mmol) and triethylamine (0.360 mL, 2.58 mmol) were added to a solution of 3-iodobenzyl alcohol 15 (0.27 mL, 2.13 mmol) and methyl acrylate 16 (0.220 mL, 2.44 mmol) in CH3CN (4.5 mL). The reaction vessel was sealed with a Teflon screw-cap and was heated at 100° C. for 5 h. At this time, the reaction was allowed to cool to room temperature and the tube was charged with 0.22 mL more of methyl acrylate, 11.7 mg Pd(OAc)2 and 0.360 mL triethylamine. The reaction was heated at 100° C. overnight and then 10 mL saturated ammonium chloride solution was added. The resulting mixture was extracted with dichloromethane (3×40 mL) and the combined dichloromethane solution was dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (30% ethyl acetate/hexanes) gave 395 mg (97%) of compound 17.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732443B2
出典データセットuspto-grants-2010_06
ORD IDord-a51aab874b354bb2a3c422fc2effc228
出典メモuspto-grants-2010_06