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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1292638생성일: 2026년 10월 25일

Sodium Chloride → 1-((2R,5R)-2,5-dimethylpyrrolidinyl)-2-diphenylphosphinylnaphthalene

https://huagongshe.com/reaction/1292638

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Lithium amideHCID 24532—
반응물2,5-Dimethylpyrrolidine, (2R,5R)-HCID 641767—
반응물Phosphine oxide, (1-methoxy-2-naphthalenyl)diphenyl-HCID 10872037—
반응물Carbon dioxide methanolHCID 21973728—
반응물Carbontetrachloride dry-iceHCID 86602444—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-((2R,5R)-2,5-dimethylpyrrolidinyl)-2-diphenylphosphinylnaphthaleneHCID 5413139369.2%

반응 조건

온도0 °C

반응 단계

In a 300 ml four-necked flask was charged 1.1 g (11 mmol) of (2R,5R)-2,5-dimethylpyrrolidine in a nitrogen stream, and 70 ml of tetrahydrofuran (THF) was added thereto. To the flask was added dropwise 7.7 ml (13.2 mmol) of butyl lithium at -78° C. (methanol-dry ice) over 10 minutes. After maintaining the system at that temperature for 10 minutes, the mixture was stirred at 0° C. for 1 hour to prepare lithium amide. In a separate container 4 g (11 mmol) of 1-methoxy-2-diphenylphosphinylnaphthalene was dissolved in 35 ml of THF, and the lithium amide was slowly added dropwise to the resulting solution cooled to -20° C. (carbon tetrachloride-dry ice), followed by allowing the mixture to react for 4 hours. The reaction was stopped by addition of a saturated sodium chloride aqueous solution, and the reaction mixture was extracted with ethyl ether. The extract was washed with water and dried over anhydrous magnesium sulfate. The resulting crude product was purified by silica gel column chromatography using a 1/1 (by volume) mixture of hexane and acetone as an eluent to give 3.24 g of 1-((2R,5R)-2,5-dimethylpyrrolidinyl)-2-diphenylphosphinylnaphthalene in a yield of 69%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05756760
출처 데이터셋uspto-grants-1998_05
ORD IDord-dd8f145013e64996be7ceaa714f7f401
출처 메모uspto-grants-1998_05