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HRID 62837作成日:2026年10月24日

Benzaldehyde, 4-(phenylmethoxy)- → (E)-Ethyl 3-(4-(benzyloxy)phenyl)-2-methylacrylate

https://huagongshe.com/ja/reaction/62837

反応式

関与物質

役割名称HCID仕込み量
反応物Benzaldehyde, 4-(phenylmethoxy)-HCID 78109—
反応物Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoateHCID 12607919—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-Ethyl 3-(4-(benzyloxy)phenyl)-2-methylacrylateHCID 1223556297.4%

反応手順

Carbethoxyethylidene triphenylphosphorane (1.02 g, 2.81 mmol) was dissolved in anhydrous THF (25 mL), and 4-benzyloxy-benzaldehyde (0.5 g, 2.36 mmol)/THF (10 mL) solution was added dropwise thereto at −78° C. The mixture was heated slowly to room temperature and then stirred for 12 hours. After the termination of the reaction, the reactant was concentrated under reduced pressure. The residue was added with water and then extracted with EtOAc. The organic layer was dried with MgSO4 and purified by column chromatography (eluent, EtOAc/Hex=1/9) to obtain the title compound (0.68 g, 97.4%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447044B2
出典データセットuspto-grants-2016_09
ORD IDord-76ce6663f0764a9fa978df089572bfa1
出典メモuspto-grants-2016_09