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HRID 2211778作成日:2026年10月27日

p-Anisoyl chloride → 4-Methoxy-N-[2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]benzamide

https://huagongshe.com/reaction/2211778

反応式

関与物質

役割名称HCID仕込み量
反応物p-Anisoyl chlorideHCID 7477—
反応物2,2,4,6,7-Pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amineHCID 10685309—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物4-Methoxy-N-[2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]benzamideHCID 1022456986%

反応手順

By using 2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amine and 4-methoxybenzoyl chloride, the title compound was synthesized according to Example 1b. Yield: 86%. Melting point: 161-163° C. (Ethyl acetate-hexane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07101867B2
出典データセットuspto-grants-2006_09
ORD IDord-f3c941257a704bc69806a5b666c0313f
出典メモuspto-grants-2006_09