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HRID 2211779作成日:2026年10月26日

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

https://huagongshe.com/reaction/2211779

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methoxy-N-[2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]benzamideHCID 10224569—
溶媒EthanolHCID 702—
生成物N-(4-Methoxybenzyl)-2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amineHCID 980196558%

反応手順

By using 4-methoxy-N-[2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]benzamide, the title compound was synthesized according to Example 2b. Yield: 58%. Melting point: 97-98° C. (Ethanol).

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-1f00a842a4a0411091b803afb1e15773
出典メモuspto-grants-2006_09