Water → 2-Amino-4-(4-ethylphenyl)-5-phenyl-3-furancarbonitrile
반응식
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9](=O)[CH:10]([OH:17])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:5][CH:4]=1)[CH3:2].[C:19](#[N:23])[CH2:20][C:21]#[N:22].C(NCC)C.O>CN(C=O)C>[NH2:23][C:19]1[O:17][C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:9]([C:6]2[CH:7]=[CH:8][C:3]([CH2:1][CH3:2])=[CH:4][CH:5]=2)[C:20]=1[C:21]#[N:22]참가 물질
실험 절차
Cool a mixture of 145 g (603 mmol) 1-(4-ethylphenyl)-2-hydroxy-2-phenylethanone and 51.8 g (784.4 mmol) malononitrile in 2.23 litres DMF to 0° C. and add 53.7 ml (518 mmol) diethylamine, with cooling. After 1 h, heat the reaction mixture to RT and stir for a further 4 h, before adding 1.5 litre water. After 30 min, pour off a large proportion of the water and replace with 750 ml of fresh water. Stir the mixture vigorously, before decanting from the sticky organic residue. Dissolve the residue in ethyl acetate, dry, and concentrate under vacuum, until the product begins to crystallize. Add 450 ml diisopropyl ether, stir and then leave to stand overnight. Filter off the crystalline precipitate with suction, wash twice with 50 ml diisopropyl ether and dry under vacuum. 98.5 g (56.6% of theor.) of the target product is obtained.
후처리
- temperatureCool
- temperaturewith cooling
- waitAfter 30 min
- stirringStir the mixture vigorously
- custombefore decanting from the sticky organic residue
- dissolutionDissolve the residue in ethyl acetate
- customdry
- concentrationconcentrate under vacuum, until the product
- customto crystallize
- additionAdd 450 ml diisopropyl ether
- stirringstir
- customleave
- waitto stand overnight
- filtrationFilter off the crystalline precipitate with suction
- washwash twice with 50 ml diisopropyl ether
- customdry under vacuum
- custom98.5 g (56.6% of theor.) of the target product is obtained
출처 및 근거
- ORD 기록
- ord-e8fc03077b3e40978b4ce3785b4bfa1e
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08183246B2
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