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HRID 43346作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/43346

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 for 3 days and then the solvent removed in vacuo. The residue was diluted with DCM, hexane was added and the resultant white precipitate filtered off. The filtrate was concentrated in vacuo and purified by 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US08536182B2
出典データセットuspto-grants-2013_09
ORD IDord-93e31a61c21a41989b70d85c7f8821d7
出典メモuspto-grants-2013_09