반응식
Cl.[CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[C:12]([CH2:14][N:15]1[CH:19]=[CH:18][N:17]=[CH:16]1)=[O:13].[CH2:20](O)[CH2:21][OH:22].O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)([O-])[O-].[K+].[K+]>C(OCC)(=O)C.C1(C)C=CC=CC=1>[CH2:20]1[CH2:21][O:22][C:12]([C:3]2[CH:4]=[CH:5][C:6]3[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=3)[CH:2]=2)([CH2:14][N:15]2[CH:19]=[CH:18][N:17]=[CH:16]2)[O:13]1참가 물질
실험 절차
A mixture of 5.45 g. of 1-(2-naphthoylmethyl)imidazole hydrochloride, 2.49 g. ethylene glycol and 7.6 g. p-toluenesulfonic acid monohydrate in 50 ml. of toluene is heated overnight under reflux through a Dean-Stark trap. The trap is then replaced by a separatory funnel containing 4 A molecular seives and heating is continued for a further day. After cooling, the mixture is treated with 200 ml. of ethyl acetate, neutralized by pouring into excess aqueous potassium carbonate and the organic phase separated and dried (MgSO4) to afford a solution of 1-[2,2-ethylenedioxy-2-(2-naphthyl)ethyl]imidazole. The hydrochloride salt is prepared by dropwise addition of ethereal hydrogen chloride until precipitation is complete. Filtration and recrystallization from acetone/methanol gives 3.9 g. pure hydrochloride. m.p. 269°-270° C.
후처리
- additionA mixture of 5.45 g
- temperatureunder reflux through a Dean-Stark trap
- customThe trap is then replaced by a separatory funnel
- additioncontaining 4 A molecular seives
- temperatureheating
- waitis continued for a further day
- temperatureAfter cooling
- additionthe mixture is treated with 200 ml
- customthe organic phase separated
- dry with materialdried (MgSO4)
출처 및 근거
- ORD 기록
- ord-f5f7466ae81b4ad3bd899d47583d00e1
- 출처 데이터셋
- uspto-grants-1979_04
- 특허 번호
- US04150153
연결된 노트
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