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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1440849생성일: 2026년 10월 24일

Dimethylformamide → 5-acetyl-3-(N-allyl-N-n-propylamino)chroman

https://huagongshe.com/ko/reaction/1440849

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TetramethyltinHCID 11661—
반응물Lithium ChlorideHCID 433294—
반응물3-(N-Allyl-N-n-propylamino)-5-trifluoromethane-sulfonyloxychromanHCID 19028220—
촉매Palladium ChlorideHCID 24290—
용매Tetrahydrofuran hexaneHCID 21883165—
생성물5-acetyl-3-(N-allyl-N-n-propylamino)chromanHCID 1902808939%

반응 조건

온도120 °C

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 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 arm) 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05500425
출처 데이터셋uspto-grants-1996_03
ORD IDord-526ef5d686dd4886b50ee5479083d2e4
출처 메모uspto-grants-1996_03