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HRID 430039作成日:2026年10月24日

Toluene → Methyl 2-(perfluoro-1-butanesulfonyloxy)-1-napthoate

https://huagongshe.com/ja/reaction/430039

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物TriethylamineHCID 8471—
反応物Perfluoro-1-butanesulfonyl fluorideHCID 67814—
反応物Methyl 2-hydroxy-1-naphthoateHCID 598533—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-(perfluoro-1-butanesulfonyloxy)-1-napthoateHCID 18353806—

反応条件

温度0 °C

反応手順

Perfluoro-1-butanesulfonyl fluoride (19 mL, 106 mmol, 1 eq) was added to a solution of methyl 2-hydroxy-1-naphthoate (21.25 g, 105 mmol, 1 eq) and triethylamine (15 mL, 108 mmol, 1 eq) in tetrahydrofuran (150 mL) maintained at an internal temperature about 0° C., under nitrogen. Once the addition was complete, the mixture was allowed to warm to ambient temperature and stirred for 64 hours. Toluene (150 mL) was added causing some precipitation. The solids were removed by filtration through Celiteä and washed with toluene (20 mL). The organic solutions were combined and washed with 2 N HCl (aq) (2×50 mL), water (100 mL), saturated aqueous sodium carbonate solution (100 mL) and brine (100 mL). The organic layer was dried (MgSO4), filtered and concentrated under reduced pressure. Yield 48.79 g, 95%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06320068B1
出典データセットuspto-grants-2001_11
ORD IDord-0b6ac454dd9f4f31a52a4a5d6e0de927
出典メモuspto-grants-2001_11