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HRID 26189作成日:2026年10月27日

Ethanol → HCID 21324990、化合物

https://huagongshe.com/reaction/26189

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Morpholine, hydrochloride (1:1)HCID 197884—
反応物Sodium BicarbonateHCID 516892—
反応物6-Methoxy-5-nitro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 13067337—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物HCID 21324990HCID 21324990—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04148897
出典データセットuspto-grants-1979_04
ORD IDord-eebd0246bce042a592c82726ed11085e
出典メモuspto-grants-1979_04