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HRID 54033作成日:2026年10月24日

Water → (S)-ibuprofen N-octyl-D-glucamine salt

https://huagongshe.com/ja/reaction/54033

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ibuprofen, (+-)-HCID 3672—
反応物1-Deoxy-1-(octylamino)-D-glucitolHCID 90064—
溶媒TolueneHCID 1140—
生成物(S)-ibuprofen N-octyl-D-glucamine saltHCID 131719976—

反応条件

温度75 °C

反応手順

Second resolution. The racemic ibuprofen from the previous step and fresh racemic ibuprofen (5.8 g) were dissolved in toluene (150 mL), and water (0.5 mL) and N-octyl-D-glucamine (12.12 g, 41 mmol) were added to the solution. This mixture was heated to 75° C., forming a clear solution, and the solution cooled to 20° C. over 4 hours. The resulting precipitate was recovered by filtration, washed with toluene (50 mL), and dried to give (S)-ibuprofen N-octyl-D-glucamine salt (13.85 g). The (S)-ibuprofen N-octyl-D-glucamine salt was stirred with water (50 mL) and KOH (2.2 g) at 45° C. for one hour, and the mixture then cooled to 15° C. The resulting precipitate was recovered by filtration, washed with water (50 mL), and dried to give N-octyl-D-glucamine (7.3 g) for recycle. The aqueous filtrate from recovery of the N-octyl-D-glucamine was acidified with 3N HCl to pH<1. The resulting precipitate was recovered by filtration to give (S)-ibuprofen (5.35 g, 58% yield, MR=50.5°-51° C., 99% ee).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621140
出典データセットuspto-grants-1997_04
ORD IDord-6470614f2d8c4a32826a822b5b59b05f
出典メモuspto-grants-1997_04