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HRID 238613作成日:2026年10月24日

[6-Chloro-4-(4-methanesulfonyl-phenoxy)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester → [4-(4-Methanesulfonyl-phenoxy)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester

https://huagongshe.com/ja/reaction/238613

反応式

関与物質

役割名称HCID仕込み量
反応物[6-Chloro-4-(4-methanesulfonyl-phenoxy)-3-methyl-naphthalen-2-yl]-acetic acid methyl esterHCID 59326613—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物[4-(4-Methanesulfonyl-phenoxy)-3-methyl-naphthalen-2-yl]-acetic acid methyl esterHCID 5932648968%

反応手順

To a solution of [6-chloro-4-(4-methanesulfonyl-phenoxy)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester (110 mg, 0.26 mmol) in methanol (3 mL) was added 10% palladium on carbon (10 mg). The resulting mixture was vigorously stirred at room temperature overnight under a hydrogen atmosphere (balloon) and then filtered. The filtrate was concentrated in vacuo to give [4-(4-methanesulfonyl-phenoxy)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester (68 mg, 67%) as a colorless oil which was directly used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642629B2
出典データセットuspto-grants-2014_02
ORD IDord-932d0f3023c341b399c673e0a2378596
出典メモuspto-grants-2014_02