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

온도

0 °C

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%.

1. additionwas added
2. temperatureAfter maintaining the system at that temperature for 10 minutes
3. customto react for 4 hours
4. extractionthe reaction mixture was extracted with ethyl ether
5. washThe extract was washed with water
6. dry with materialdried over anhydrous magnesium sulfate
7. customThe resulting crude product was purified by silica gel column chromatography
8. additiona 1/1 (by volume) mixture of hexane and acetone as an eluent

ORD 기록

ord-dd8f145013e64996be7ceaa714f7f401

출처 데이터셋

uspto-grants-1998_05

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05756760