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HRID 883768作成日:2026年10月26日

3-Fluorophenol → Tert-butyl 4-(3-fluorophenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/883768

反応式

関与物質

役割名称HCID仕込み量
反応物3-FluorophenolHCID 9743—
反応物TriphenylphosphineHCID 11776—
反応物Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-(3-fluorophenoxy)piperidine-1-carboxylateHCID 5769952094.1%

反応手順

To a solution of 1,1-dimethylethyl 4-hydroxy-1-piperidinecarboxylate (24 g, 112 mmol), 3-fluorophenol (5.6 g, 59 mmol) and triphenylphosphine (31.4 g, 118 mmol) in THF (100 ml) was added di-isopropylazodicarboxylate (23.3 ml, 118 mmol). The reaction was stirred at room temperature over-weekend and then the solvent was removed in vacuo. The residue was diluted with DCM, hexane was added and the resultant precipitate was filtered off. The filtrate was concentrated in vacuo and purified by column chromatography. Elution with DCM gave the title compound (16.4 g, 87% pure). δH (CDCl3, 250 MHz) 1.47 (9H, s), 1.76 (2H, m), 1.92 (2H, m), 3.35 (2H, ddd), 3.69 (2H, ddd), 4.44 (1H, m), 6.65 (3H, m), 7.20 (1H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236953B2
出典データセットuspto-grants-2012_08
ORD IDord-abcee7d6c32b4feab2c52658dd001a1a
出典メモuspto-grants-2012_08