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HRID 1259582作成日:2026年10月25日

3,4-Dichlorophenol → 3-(4,5-dichloro-2-hydroxyphenyl)-3-hydroxy-1-pentyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1259582

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-DichlorophenolHCID 7258—
反応物SesamolHCID 68289—
反応物1-Pentyl-1H-indole-2,3-dioneHCID 1581092—
反応物4-bromo-1-pentyl-1H-indole-2,3-dioneHCID 28492458—
生成物3-(4,5-dichloro-2-hydroxyphenyl)-3-hydroxy-1-pentyl-1,3-dihydro-2H-indol-2-oneHCID 58872503—

反応手順

Following the procedure as described in PREPARATION 1C, and making non-critical variations to replace 4-bromo-1-pentyl-1H-indole-2,3-dione with 1-pentyl-1H-indole-2,3-dione, and 1,3-benzodioxol-5-ol with 3,4-dichlorophenol, the title compound was obtained (26%): 1H NMR (300 MHz, CDCl3) δ 9.60 (s, 1H), 7.50-7.40 (m, 2H), 7.22 (td, 1H), 7.11 (s, 1H), 6.95 (d, 1H), 6.86 (s, 1H), 4.31-4.12 (br, 1H), 3.79-3.59 (m, 2H), 1.76-1.62 (m, 2H), 1.40-1.27 (m, 4H), 0.88 (t, 3H); MS (ES+) m/z 363 (M−17), 403 (M+23).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08466188B2
出典データセットuspto-grants-2013_06
ORD IDord-a542fe1301314bada72bd180543310aa
出典メモuspto-grants-2013_06