{"title":"金属镍/锌/水/乙醇催化不饱和酯的氢化反应","authors":"睦司 酒井, 政史 出口, 浩司 東","doi":"10.1246/NIKKASHI.2002.239","DOIUrl":null,"url":null,"abstract":"Under nitrogen atmosphere diethyl maleate was hydrogenated to give diethyl succinate in a high yield with metallic nickel/Zn/H2O/EtOH catalyst system in the presence of a large amount of zinc powder and water. Metallic nickel was an active species for the hydrogenation and zinc powder and water were reagents to produce hydrogen. Benzylideneaniline was hydrogenated to give N-phenylbenzylamine in a moderate yield under the reaction conditions and it was appreciably hydrolyzed to afford aniline and benzaldehyde at the same time.","PeriodicalId":19311,"journal":{"name":"Nippon Kagaku Kaishi","volume":"54 1","pages":"239-241"},"PeriodicalIF":0.0000,"publicationDate":"2002-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"金属ニッケル/亜鉛/水/エタノール触媒系による不飽和エステルの水素化反応\",\"authors\":\"睦司 酒井, 政史 出口, 浩司 東\",\"doi\":\"10.1246/NIKKASHI.2002.239\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Under nitrogen atmosphere diethyl maleate was hydrogenated to give diethyl succinate in a high yield with metallic nickel/Zn/H2O/EtOH catalyst system in the presence of a large amount of zinc powder and water. Metallic nickel was an active species for the hydrogenation and zinc powder and water were reagents to produce hydrogen. Benzylideneaniline was hydrogenated to give N-phenylbenzylamine in a moderate yield under the reaction conditions and it was appreciably hydrolyzed to afford aniline and benzaldehyde at the same time.\",\"PeriodicalId\":19311,\"journal\":{\"name\":\"Nippon Kagaku Kaishi\",\"volume\":\"54 1\",\"pages\":\"239-241\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-02-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nippon Kagaku Kaishi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1246/NIKKASHI.2002.239\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nippon Kagaku Kaishi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1246/NIKKASHI.2002.239","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Under nitrogen atmosphere diethyl maleate was hydrogenated to give diethyl succinate in a high yield with metallic nickel/Zn/H2O/EtOH catalyst system in the presence of a large amount of zinc powder and water. Metallic nickel was an active species for the hydrogenation and zinc powder and water were reagents to produce hydrogen. Benzylideneaniline was hydrogenated to give N-phenylbenzylamine in a moderate yield under the reaction conditions and it was appreciably hydrolyzed to afford aniline and benzaldehyde at the same time.
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