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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290340생성일: 2026년 10월 24일

Sodium Acetate → Nabumetone

https://huagongshe.com/reaction/1290340

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AcetateHCID 517045—
반응물Acetic acid, sodium salt, monohydrateHCID 23681166—
반응물4-(5-Bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-oneHCID 70179405—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물NabumetoneHCID 440952.6%

반응 조건

온도60 °C

반응 단계

48 Grams (0.150 moles) of 4-(5-bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-one, 6.1 g of sodium acetate hydrate containing 32.4% of water, equivalent to 0.050 moles of sodium acetate, 4 g of a 50% suspension in water of 10% palladium on carbon, equivalent to 0.0019 moles of palladium, and 500 ml of methanol are put in a hydrogenator. The hydrogenator is washed with nitrogen in order to eliminate the oxygen and then hydrogen is introduced at the pressure of 2 atmospheres. The temperature of reaction is kept at 40° C. for a period of time of 6 hours, then the hydrogen is let off, the hydrogenator is washed with nitrogen and the reaction mixture is filtered to eliminate the catalyst. The solution is brought to pH 6 with a 5% aqueous solution of sodium hydroxide and concentrated under vacuum. The oily residue is dissolved into 130 ml of isopropanol and 30 ml of N,N-dimethylformamide and the solution is added with 45 ml of water and 17.6 g of sodium bisulfite obtaining a suspension that is stirred for one hour at 60° C., then is cooled to 5° C. and is filtered. The obtained solid is washed with 75 ml of methanol, suspended in 200 ml of a 5% aqueous solution of sodium hydroxide and kept under stirring at room temperature for three hours. The suspension is then filtered, the solid is washed with water until neutrality and dried in oven under vacuum obtaining 18 g of product with a yield equal to 52.8%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05750793
출처 데이터셋uspto-grants-1998_05
ORD IDord-8a6929cd566b4773813b1c5e61f98a4e
출처 메모uspto-grants-1998_05