참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | Lithium amide | HCID 24532 | — |
| 반응물 | 2,5-Dimethylpyrrolidine, (2R,5R)- | HCID 641767 | — |
| 반응물 | Phosphine oxide, (1-methoxy-2-naphthalenyl)diphenyl- | HCID 10872037 | — |
| 반응물 | Carbon dioxide methanol | HCID 21973728 | — |
| 반응물 | Carbontetrachloride dry-ice | HCID 86602444 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-((2R,5R)-2,5-dimethylpyrrolidinyl)-2-diphenylphosphinylnaphthalene | HCID 54131393 | 69.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05756760 |
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| 출처 데이터셋 | uspto-grants-1998_05 |
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| ORD ID | ord-dd8f145013e64996be7ceaa714f7f401 |
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| 출처 메모 | uspto-grants-1998_05 |
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