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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26189생성일: 2026년 10월 26일

Ethanol → HCID 21324990, 화합물

https://huagongshe.com/reaction/26189

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Morpholine, hydrochloride (1:1)HCID 197884—
반응물Sodium BicarbonateHCID 516892—
반응물6-Methoxy-5-nitro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 13067337—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물HCID 21324990HCID 21324990—

반응 단계

In 100 ml. of ethanol is dissolved a mixture of 1 g. of 6-methoxy-5-nitro-3,4-dihydro-1(2H)-naphthalenone and 3 g. of morpholine hydrochloride and the mixed solution is reacted at 80° C. for 10 hours. The reaction mixture is cooled and, following addition of 500 ml. of water, it is shaken with 100 ml. of diethyl ether. The water layer is neutralized with sodium hydrogen carbonate and extracted with chloroform. The extract is dried and distilled under reduced pressure to remove the solvent. By the above procedure is obtained 6-methoxy-2-morpholinomethyl-5-nitro-3,4-dihydro-1(2H)-naphthalenone as an oily product. This product is dissolved in 50 ml. of methanol and, after addition of 1 g. of sodium borohydride, the solution is stirred at room temperature for 30 minutes. To this reaction mixture is added 500 ml. of water and the mixture is extracted with chloroform. The extract is dried and distilled under reduced pressure to remove the solvent. The above procedure provides an oil of 6-methoxy-2-morpholinomethyl-5-nitro-1,2,3,4-tetrahydro-1-naphthalenol. This product is dissolved in 20 ml. of ethanolic hydrochloric acid and the solution is heated at 80° C. for 1 hour. Following the addition of 50 ml. of ethyl acetate, the solution is cooled, whereupon 0.35 g. of 7-methoxy-3-morpholinomethyl-8-nitro-1,2-dihydronaphthalene hydrochloride is obtained as pale-yellow prisms melting at 200°-270° C. (gradually decomposed).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148897
출처 데이터셋uspto-grants-1979_04
ORD IDord-eebd0246bce042a592c82726ed11085e
출처 메모uspto-grants-1979_04