참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Tetramethyltin | HCID 11661 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | 3-(N-Allyl-N-n-propylamino)-5-trifluoromethane-sulfonyloxychroman | HCID 19028220 | — |
| 촉매 | Palladium Chloride | HCID 24290 | — |
| 촉매 | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| 용매 | Tetrahydrofuran hexane | HCID 21883165 | — |
| 생성물 | 5-acetyl-3-(N-allyl-N-n-propylamino)chroman | HCID 19028089 | 39% |
반응 단계
3-(N-Allyl-N-n-propylamino)-5-trifluoromethanesulfonyloxychroman (0.28 g, 0.74 mmol), LiCl (0.097 g, 2.3 mmol), PdCl2 (dppf) (0.031 g, 0.04 mmol) and 2.6-di-t-butyl-4-methylphenol (0.005 g) were dissolved in DMF (5.0 mL) in a three-necked round-bottom flask (50 mL) with a magnetic stirrer. The flask was evacuated, followed by inlet of CO (three times). Tetramethyltin (0.12 mL, 0.89 mmol) was added and then the mixture was stirred under an atmosphere of CO (1 atm) at 120° C. (oilbath temp) for 4 hours. The solvent was evaporated, the residue was partitioned between aqueous NH3 (2M) and CH2Cl2 (3×15 mL) and the organic phases were dried (Na2SO4), filtered and concentrated in vacuo. Column chromatography on silica with THF-n-hexane (1:9) as eluent afforded 5-acetyl-3-(N-allyl-N-n-propylamino)-chroman (0.078 g, 39% yield) as an oil. The base was precipitated from an ether solution by adding a slight excess of HCl (approx. 3M in ether). The crude salt was collected and dried in vacuo at 40° C. to give a white amorphous powder. Mp 125°-127° C. PdCl2 (dppf)=dichloro[1,1'-bis(diphenylphosphino)-ferrocene]-palladium (II).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05646309 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-bbae8b7c8b2e4a4c887fd126b97d206f |
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| 출처 메모 | uspto-grants-1997_07 |
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