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HRID 482113作成日:2026年10月24日

Benzenesulfonic acid 3-benzyloxy-5-methylphenyl ester → Benzenesulfonic acid 3-hydroxy-5-methylphenyl ester

https://huagongshe.com/ja/reaction/482113

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonic acid 3-benzyloxy-5-methylphenyl esterHCID 54005214—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Benzenesulfonic acid 3-hydroxy-5-methylphenyl esterHCID 1105454598.4%

反応手順

A mixture of benzenesulfonic acid 3-benzyloxy-5-methylphenyl ester (532 mg, 1.5 mmol), as prepared in the preceding step, and 10% palladium on carbon (200 mg) in ethanol (20 mL) was hydrogenated (balloon) overnight. The catalyst was removed by filtering over diatomaceous earth and the filtrate was evaporated in vacuo to give the title compound as a colorless syrup (390 mg, 98%). 1H-NMR (300 MHz, CDCl3 /CD3OD) δ 2.19 (s, 3H), 6.27 (s, 1H), 6.54 (s, 1H), 6.66 (s 1H), 7.43 (m, 1H), 7.55 (t, 1H), 7.70 (t, 1H), 7.85 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05792769
出典データセットuspto-grants-1998_08
ORD IDord-07fbf5c563664a749808f9942eb4a60d
出典メモuspto-grants-1998_08