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HRID 1372750作成日:2026年10月25日

1-Naphthaldehyde → Methyl (2-(1-naphthyl)-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372750

反応式

関与物質

役割名称HCID仕込み量
反応物1-NaphthaldehydeHCID 6195—
反応物Iodo benzene diacetateHCID 12217721—
反応物Methyl 2-(4-amino-3-hydroxyphenyl)acetateHCID 17858854—
溶媒EthanolHCID 702—
生成物Methyl (2-(1-naphthyl)-6-benzoxazolyl)acetateHCID 5877844042%

反応手順

In EtOH (8 ml), 1-naphthaldehyde (263 mg, 1.68 mmol) and methyl 4-amino-3-hydroxyphenylacetate (305 mg, 1.68 mmol) were stirred at room temperature for 12 hours. Iodobenzene diacetate (651 mg, 2.02 mmol) was added to the reaction mixture, followed by stirring at room temperature for 5 minutes. After removal of the solvent by distilling the reaction mixture under reduced pressure, the residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (6:1, v/v) eluate fractions, methyl (2-(1-naphthyl)-6-benzoxazolyl)acetate (223 mg, 42%) was obtained as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157487B2
出典データセットuspto-grants-2007_01
ORD IDord-90e088c89fe94f72af7c19ed60ce651e
出典メモuspto-grants-2007_01