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HRID 1636504作成日:2026年10月27日

2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl ester → 2-Chlorobenzenesulfonic acid 3-hydroxyphenyl ester

https://huagongshe.com/reaction/1636504

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl esterHCID 54263647—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
生成物2-Chlorobenzenesulfonic acid 3-hydroxyphenyl esterHCID 5401528196.6%

反応手順

2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl ester (3.75 g, 10 mmol), as prepared in the preceding step, Pd/C (10%) (350 mg) in tetrahydrofuran (80 mL) was hydrogenated balloon) for 3 h. The catalyst was filtered through Celite and washed with tetrahydrofuran. The combined tetrahydrofuran solution was evaporated in vacuo and the residue was then purified by flash column chromatography (methylene chloride) to give the title compound as a colorless oil (2.75 g, 95%). 1H-NMR (300 MHz, CDCl3) δ 6.68 (m, 3H), 7.12 (t, 1H, J=6.5 Hz), 7.37 (t, 1H, J=7.1 Hz), 7.60 (m, 2H), 7.94 (dd, 1H, J=0.6, 4.0 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06034127
出典データセットuspto-grants-2000_03
ORD IDord-419e35e221ba4e549739011ad3e56805
出典メモuspto-grants-2000_03