戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 217088作成日:2026年10月25日

Hydrochloric Acid → 22-Hydroxydocosanoic acid

https://huagongshe.com/reaction/217088

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Hydrogen PeroxideHCID 784—
反応物Sodium HydroxideHCID 14798—
反応物Docos-21-enoic acid ethyl esterHCID 86625390—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物22-Hydroxydocosanoic acidHCID 5282922—

反応条件

温度0 °C

反応手順

22-Hydroxy-docosanoic acid was synthesized according to Mori et al., Liebigs Ann. Chem., (1991), 253-257. Briefly, under N2 atmosphere 6.6 g Docos-21-enoic acid ethyl ester and 30 ml THF were combined and cooled down to 0° C. Then 0.5 eq. (9 ml) borane/THF complex was added dropwise and the mixture was allowed to stir for 2 hours at room temperature. After the addition of 1.2 ml H2O the suspension was again cooled down to 0° C. and 15 ml 3M NaOH and 2 ml 35% H2O2 were added. The mixture was stirred for one hour at 50° C. Then the temperature was brought to room temperature and the pH was adjusted to pH 2-3 with 2N HCl. The solid was fritted, washed with H2O, codistilled three times with CHCl3 and recrystallized from CHCl3. After a further treatment with NaOH (3M in H2O) in THF at 50° C. over 1.5 days the pH was again adjusted to pH 2-3 and the crude product was fritted, washed with H2O and codistilled two times with CHCl3. The product was characterized by thin layer chromatography and 1H-NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193246B2
出典データセットuspto-grants-2012_06
ORD IDord-04862cbc8f40475e9a9b4c04188ddee9
出典メモuspto-grants-2012_06