戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7218作成日:2026年10月24日

Hydrochloric Acid → Tert-butyl 3-hydroxy-3-phenyl-3-(pyridin-2-yl)propionate

https://huagongshe.com/ja/reaction/7218

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PyridineHCID 1049—
反応物2-BenzoylpyridineHCID 7038—
反応物TetrahydrofuranHCID 8028—
反応物CinchonineHCID 90454—
生成物Tert-butyl 3-hydroxy-3-phenyl-3-(pyridin-2-yl)propionateHCID 1215030998%

反応条件

温度-40 °C

反応手順

Under argon atmosphere, cinchonine (440 mg, 1.0 mmol) was suspended in tetrahydrofuran (absolute, 2.0 mL), and to this suspension was added a Reformatsky reagent (0.5 M; 8.0 mL, 4.0 mmol) dropwise under ice-cooling. After stirring for 10 minutes, pyridine (0.30 mL, 2 mmol) was added thereto dropwise. After stirring for 20 minutes under ice-cooling, the mixture was cooled to −40° C. A solution of 2-benzoylpyridine (183 mg, 1.0 mmol) in tetrahydrofuran (absolute, 4.0 mL) was added dropwise over 10 minutes, and the mixture was stirred at −40° C. for 4 hours. To this reaction solution was added 1N HCl (20 mL), which was then extracted with ethyl acetate (20 mL×2). The extracted solution was washed successively with an aqueous saturated sodium bicarbonate solution and an aqueous saturated sodium chloride solution. After the organic layer was dried with sodium sulfate, the solvent was removed under reduced pressure. The residue was analyzed with high performance liquid chromatography. Consequently, the yield was 98% and the enantiomer excess was 90%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084278B2
出典データセットuspto-grants-2006_08
ORD IDord-83ed61dbe4a343a899a0eeb5417de98f
出典メモuspto-grants-2006_08