{"title":"月桂叶氯仿提取物的植物化学分析","authors":"D. P. Pandey, S. Saxena","doi":"10.51129/ujpah-2022-33-2(6)","DOIUrl":null,"url":null,"abstract":"The air-dried and powdered leaves (3 kg) of Skimmia laureola were exhaustively defatted with light petroleum ether (60-800). The petroleum free mass extracted with 90% ethanol. The ethanol extract was concentrated under reduced pressure and a suspension of the residue was made with water, which was washed with diethyl ether for several times and then partitioned with CHCl3:H2O:MeOH (6:4:4) in a separatory funnel. The chloroform layer was separated out and concentrated under reduced pressure to give CHCl3 extract (15g). The chloroform extract (10g) was subjected to repeated CC over Si-gel eluted with different proportions of n-hexane- CHCl3 and CHCl3:MeOH afforded β-stosterol (1), (E)-3’-(4-Hydroxyphenyl)-2’-propenoic methyl ester (2), (E)-3’-(4-Hydroxy-3-methoxyphenyl)-2’-propenoic methyl ester (3), Identified as bergapten (4), Identification of these compounds were made by the analysis of their chemical and spectral data.","PeriodicalId":432227,"journal":{"name":"Universities' Journal of Phytochemistry and Ayurvedic Heights","volume":"44 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phytochemical analysis of chloroform extract of leaves of Skimmia laureola\",\"authors\":\"D. P. Pandey, S. Saxena\",\"doi\":\"10.51129/ujpah-2022-33-2(6)\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The air-dried and powdered leaves (3 kg) of Skimmia laureola were exhaustively defatted with light petroleum ether (60-800). The petroleum free mass extracted with 90% ethanol. The ethanol extract was concentrated under reduced pressure and a suspension of the residue was made with water, which was washed with diethyl ether for several times and then partitioned with CHCl3:H2O:MeOH (6:4:4) in a separatory funnel. The chloroform layer was separated out and concentrated under reduced pressure to give CHCl3 extract (15g). The chloroform extract (10g) was subjected to repeated CC over Si-gel eluted with different proportions of n-hexane- CHCl3 and CHCl3:MeOH afforded β-stosterol (1), (E)-3’-(4-Hydroxyphenyl)-2’-propenoic methyl ester (2), (E)-3’-(4-Hydroxy-3-methoxyphenyl)-2’-propenoic methyl ester (3), Identified as bergapten (4), Identification of these compounds were made by the analysis of their chemical and spectral data.\",\"PeriodicalId\":432227,\"journal\":{\"name\":\"Universities' Journal of Phytochemistry and Ayurvedic Heights\",\"volume\":\"44 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Universities' Journal of Phytochemistry and Ayurvedic Heights\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.51129/ujpah-2022-33-2(6)\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Universities' Journal of Phytochemistry and Ayurvedic Heights","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51129/ujpah-2022-33-2(6)","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Phytochemical analysis of chloroform extract of leaves of Skimmia laureola
The air-dried and powdered leaves (3 kg) of Skimmia laureola were exhaustively defatted with light petroleum ether (60-800). The petroleum free mass extracted with 90% ethanol. The ethanol extract was concentrated under reduced pressure and a suspension of the residue was made with water, which was washed with diethyl ether for several times and then partitioned with CHCl3:H2O:MeOH (6:4:4) in a separatory funnel. The chloroform layer was separated out and concentrated under reduced pressure to give CHCl3 extract (15g). The chloroform extract (10g) was subjected to repeated CC over Si-gel eluted with different proportions of n-hexane- CHCl3 and CHCl3:MeOH afforded β-stosterol (1), (E)-3’-(4-Hydroxyphenyl)-2’-propenoic methyl ester (2), (E)-3’-(4-Hydroxy-3-methoxyphenyl)-2’-propenoic methyl ester (3), Identified as bergapten (4), Identification of these compounds were made by the analysis of their chemical and spectral data.