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HRID 2226281생성일: 2026년 10월 26일

Benzaldehyde → N,N-diethyl-5-phenyl-5-hydroxy-3-oxopentanamide

https://huagongshe.com/reaction/2226281

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Hydrochloric AcidHCID 313—
반응물Acetoacetamide, N,N-diethyl-HCID 16699—
반응물Sodium hydrideHCID 24758—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물N,N-diethyl-5-phenyl-5-hydroxy-3-oxopentanamideHCID 1896727197.7%

반응 조건

온도-10 °C

반응 단계

1.53 g of 80% sodium hydride (51.0 mmol) in 60 cm3 of tetrahydrofuran are introduced into a three-necked, round-bottomed flash equipped with a septum and a dropping funnel. The mixture is cooled to -10° C. and then 5.5 g of 97% N,N-diethylacetoacetamide (34.0 mmol) are slowly added. The mixture is stirred for 15 minutes. 21.25 cm3 of n-butyllithium in solution in hexane at 1.6 mol/liter are then slowly added and the mixture is then stirred for 15 minutes. 3.05 g of benzaldehyde (28.5 mmol) are introduced. The mixture is stirred for 25 minutes and then 6 cm3 of concentrated hydrochloric acid and 35 cm3 of water are added. Extraction is carried out with 3 times 25 cm3 of dichloromethane. The combined organic phases are washed with 2 times 100 cm3 of water and dried over sodium sulphate. After filtration and concentration to dryness under reduced pressure, there is obtained, with a yield of 97.7%, 7.33 g of N,N-diethyl -5-phenyl-5-hydroxy-3-oxopentanamide, the structure of which is confirmed by the proton nuclear magnetic resonance spectrum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05347039
출처 데이터셋uspto-grants-1994_09
ORD IDord-21ed734c48a043b39f59a427eaeb24c8
출처 메모uspto-grants-1994_09