戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 54496作成日:2026年10月26日

Benzyl Alcohol → p-Toluenesulfonic acid

https://huagongshe.com/reaction/54496

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物Pipecolic acid, (-)-HCID 439227—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物2,3-DihydroxybutanedioateHCID 3806114—
溶媒BenzeneHCID 241—
溶媒Diethyl EtherHCID 3283—
生成物p-Toluenesulfonic acidHCID 6101185.5%

反応手順

To a slurry of 7.3 g (26.14 mmol) of the tartrate salt of (S)-pipecolic acid (Egbertson M. and S. J. Danishefsky, J. Org. Chem. 54:11 (1989) in 75 mL of dry benzene was added 13.5 mL (0.13 mol) of benzyl alcohol and 5.48 g (28.8 mmol) of p-toluenesulfonic acid monohydrate. The reaction mixture was heated at reflux under a Dean-Stark trap for 2 h and then cooled to room temperature. The solution was then diluted with 400 mL of ether and stirred overnight at 4° C. The resulting white solid was collected on a filter, washed with hexane and dried in vacuo to give 9.2 g (90%) of the p-toluenesulfonic acid salt of benzyl pipecolate (14). 1H NMR (300 MHz, D2O) δ 7.63 (d), 7.41 (s), 7.28 (d), 5.26 (ABq), 4.8 (s), 4.03 (dd), 3.92 (dd), 3.51-3.39 (m), 3.15-2.93 (s), 2.40 (s), 2.36-2.24 (m), 1.98-1.53 (m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622970
出典データセットuspto-grants-1997_04
ORD IDord-8b1914876ed14971ac26a0132645feb3
出典メモuspto-grants-1997_04