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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2166180생성일: 2026년 10월 25일

Potassium Hydroxide → Levetiracetam

https://huagongshe.com/reaction/2166180

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참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Sodium SulfateHCID 24436—
반응물4-Chlorobutyryl chlorideHCID 78370—
반응물(2S)-2-Aminobutanamide hydrochlorideHCID 11961924—
촉매Tetrabutylammonium BromideHCID 74236—
용매DichloromethaneHCID 6344—
생성물LevetiracetamHCID 528458374.1%

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온도0 °C

반응 단계

This example illustrates a variant of the process of Example 3, in which the intermediate 4-chlorobutanamide obtained in situ is not isolated. 84 g of anhydrous sodium sulfate are added to a suspension of 69.25 g (0.5 mole) of (S)-2-amino-butanamide hydrochloride in 600 ml of dichloromethane at ambient temperature. The mixture is cooled to 0° C. and 115 g of ground potassium hydroxide are added, followed by 8.1 g (0.025 mole) of tetrabutylammonium bromide dissolved in 100 ml of dichloromethane. A solution of 77.5 g of 4-chlorobutyryl chloride in 100 ml of dichlorometha is added dropwise at 0° C., wih vigorous stirring. After 5 hours' reaction, a further 29 g of ground potassium hydroxide are added. Two hours later, the reaction mixture is filtered over Hyflo-cel and the filtrate evaporated under reduced pressure. The residue (93.5 g) is dispersed in 130 ml of hot toluene for 45 minutes. The resultant mixture is filtered and the filtrate evaporated under reduced pressure. The residue (71.3 g) is dissolved hot in 380 ml of ethyl acetate to which 23 g of 0,4 nm molecular sieve in powder form are added. This mixture is heated to reflux temperature and filtered hot. After cooling the filtrate, the desired product crystallizes to give 63 g of (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04943639
출처 데이터셋uspto-grants-1990_07
ORD IDord-8404b736d79843edb781592f477f858b
출처 메모uspto-grants-1990_07