반응 #362828
ord-86df17c6bb4741a88a27b74fcbf1ebf9
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시약
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후처리
- 1기타are placed in a three-necked flask
- 2기타which is surmounted with a dropping funnel
- 3온도maintained under a nitrogen atmosphere
- 4workup.STIRRINGAfter stirring for 19 h
- 5workup.STIRRINGthe mixture is stirred for 26 h
- 6추출this mixture is extracted with 1 l of ethyl acetate
- 7기타The aqueous phase is separated off after settling
- 8세척washed with 2 times 500 ml of ethyl acetate
- 9세척washed with 500 ml of distilled water
- 10기타separated off
- 11건조dried over magnesium sulphate
- 12여과filtered
- 13농축concentrated to dryness in order
- 14기타to yield a chestnut oil
- 15기타this oil is purified by flash chromatography (eluant, CH2Cl290/AcOEt 10) in order
실험 절차
10 g of diethyl 4-aminobenzylacetamidomalonate dissolved in 150 ml of DMF are placed in a three-necked flask which is surmounted with a dropping funnel and maintained under a nitrogen atmosphere. 6.57 ml of allyl bromide, and then 10.76 ml of triethylamine, are added slowly, at room temperature and while stirring. After stirring for 19 h, a further 1.31 ml of allylbromide and 2.15 ml of triethylamine are then added and the mixture is stirred for 26 h. The reaction medium is poured onto 1.5 l of distilled water and this mixture is extracted with 1 l of ethyl acetate. The aqueous phase is separated off after settling and washed with 2 times 500 ml of ethyl acetate. The organic phases are combined, washed with 500 ml of distilled water and then with 500 ml of water which is saturated with sodium chloride, separated off, dried over magnesium sulphate, filtered and then concentrated to dryness in order to yield a chestnut oil; this oil is purified by flash chromatography (eluant, CH2Cl290/AcOEt 10) in order to yield 6.66 g of diethyl 4-diallylaminobenzylacetamidomalonate in the form of a beige solid which melts at 94-96° C. (Rf=0.6, AcOEt 50/cyclohexane 50) and 3.49 g of diethyl 4-allylaminobenzylacetamidomalonate in the form of a beige solid which melts at 104-106° C. (Rf0.45 AcOEt 50/cyclohexane 50).