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HRID 1017900作成日：2026年10月25日

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

https://huagongshe.com/reaction/1017900

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluoro-N-(2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]benzamideHCID 10202094—
溶媒MethanolHCID 887—
生成物N-(4-Fluorobenzyl)-2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amineHCID 993102439%

反応手順

By using 4-fluoro-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: 39%. Melting point: 92-94° C. (Methanol)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479536B1
出典データセットuspto-grants-2002_11
ORD IDord-4c24fa1a939a4e4bb3824b6d9d6a68f9
出典メモuspto-grants-2002_11