戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 419313作成日:2026年10月24日

Triphenylphosphine → HCID 59452627、化合物

https://huagongshe.com/ja/reaction/419313

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-Methyl-4-nitrophenolHCID 17412—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物Benzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
溶媒DichloromethaneHCID 6344—
生成物HCID 59452627HCID 5945262787%

反応条件

温度0 °C

反応手順

3-Methyl-4-nitrophenol (1.74 g, 11.4 mmol), triphenylphosphine (5.98 g, 22.8 mmol), and phenylmethyl 4-hydroxy-1-piperidinecarboxylate (3.99 g, 17.0 mmol) were dissolved in DCM with stirring and cooled to 0° C. Diisopropyl azodicarboxylate (3.35 mL, 17.0 mmol) was added via syringe. The reaction was stirred for 10 min and allowed to warm to rt. The reaction was stirred overnight and adsorbed onto silica gel. The crude material was purified by flash chromatography, and fractions containing product were concentrated in vacuo. The material was contaminated with 3-methyl-4-nitrophenol. The material was dissolved in diethyl ether and washed with 2N NaOH solution (3×), H2O, and brine. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to provide 3.67 g (87%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ 8.02 (d, J=9.0 Hz, 1H), 7.42-7.24 (m, 5H), 7.06 (d, J=2.4 Hz, 1H), 7.01 (dd, J=9.1, 2.7 Hz, 1H), 5.07 (s, 2H), 4.76 (ddd, J=7.7, 4.2, 4.0 Hz, 1H), 3.81-3.64 (m, 2H), 3.31 (br. s., 2H), 2.52 (s, 3H), 2.01-1.88 (m, 2H), 1.63-1.49 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093239B2
出典データセットuspto-grants-2012_01
ORD IDord-d6bad6fa66c74a7881dd631728f4e66b
出典メモuspto-grants-2012_01