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HRID 1168885作成日:2026年10月25日

2,2,2-trifluoro-N-(7-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamide → 7-Propylamino-5,6,7,8-tetrahydro-naphthalen-2-ol

https://huagongshe.com/reaction/1168885

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,2-trifluoro-N-(7-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamideHCID 22560660—
溶媒MethanolHCID 887—
溶媒Sodium HydroxideHCID 14798—
生成物7-Propylamino-5,6,7,8-tetrahydro-naphthalen-2-olHCID 10058787113.5%

反応手順

A solution of 2,2,2-trifluoro-N-(7-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-acetamide (340 mg, 1.03 mmol) in methanol (30 mL) and 1N NaOH (30 mL) were stirred at room temperature for 30 h. The reaction was concentrated and the residue partitioned between EtOAc (40 mL) and water (40 mL). The aqueous layer was extracted twice more with EtOAc (2×30 mL). The combined organic layers were washed with brine (30 mL), dried (MgSO4), and concentrated to afford 7-propylamino-5,6,7,8-tetrahydro-naphthalen-2-ol (240 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06627644B2
出典データセットuspto-grants-2003_09
ORD IDord-9f60f4995a324449a7cc2163695c482a
出典メモuspto-grants-2003_09