참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | Triisopropyl borate | HCID 21531 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 2-Fluoro-6-octyloxypyridine | HCID 19046937 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | HCID 86585711 | HCID 86585711 | — |
| 생성물 | 2-Fluoro-6-octyloxypyridine-3-boronic acid | HCID 19046940 | 58.1% |
반응 단계
34.62 ml (69.24 mmol) of a 2-molar solution of lithium diisopropylamide in tetrahydrofuran/hexane/ethylbenzene are added dropwise at -78° C. to 13.00 g (57.70 mmol) of 2-fluoro-6-octyloxypyridine in 200 ml of tetrahydrofuran, and the mixture is stirred for 4 hours. 26.05 g (138.48 mmol) of triisopropyl borate are then added dropwise at -78° C., and the reaction mixture is stirred overnight, during which it warms to room temperature. After addition of 80 ml of 10% hydrochloric acid and stirring at room temperature for 1 hour, sodium chloride solution is added, the mixture is extracted with ether, the ether phase is washed with sodium chloride solution, dried over sodium sulfate, filtered and concentrated. Recrystallization from acetonitrile gives 9.03 g (33.55 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid. ##STR22##
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05630962 |
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| 출처 데이터셋 | uspto-grants-1997_05 |
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| ORD ID | ord-c38e4cfaab654911b6722d8cb1c59be2 |
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| 출처 메모 | uspto-grants-1997_05 |
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