반응식
[Cl:1][C:2]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:3]=1[O:4][CH2:5][C:6](Cl)=[O:7].CN1C=CN=C1.[N+:20]([CH:23]=[C:24]1[NH:29][CH2:28][CH2:27][CH2:26][S:25]1)([O-:22])=[O:21].[O-][Si]([O-])=O.[Mg+2]>O1CCCC1.C(Cl)Cl.O>[Cl:1][C:2]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:3]=1[O:4][CH2:5][C:6](=[O:7])[C:23]([N+:20]([O-:22])=[O:21])=[C:24]1[NH:29][CH2:28][CH2:27][CH2:26][S:25]1참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
A solution of 7.2 g of 2,4-dichlorophenoxyacetyl chloride in 20 ml of tetrahydrofuran was added dropwise to a solution of 2.5 g of 1-methylimidazole in 80 ml of tetrahydrofuran at 0.5°. The resulting slurry was stirred for 30 minutes at 5°, then 4.8 g of 5B was added all at once. The mixture was stirred overnight. Then 0.5 equivalent mole of the imidazole complex in 50 ml of tetrahydrofuran was prepared and added at 5°. The stirred mixture was allowed to rise slowly to room temperature, and stirred overnight. The solvent was stripped; the residue was treated with 1:1 volume mixture of water and methylene chloride. The phases were separated, the water phase was extracted with methylene chloride, the methylene chloride solutions were combined, washed with water and saturated salt solution, dried (MgSO4) and the solvent was stripped to give an oil. The oil was passed through Florisil to give a mush, which was triturated with pentane to give 3-(2,4-dichlorophenoxy)- 1-nitro-1-(tetrahydro-2H-1,3-thiazin-2-ylidene)-2-propanone (5C), as a pale yellow solid, m.p.: 164°-164.5°.
후처리
- stirringThe mixture was stirred overnight
- additionadded at 5°
- customto rise slowly to room temperature
- stirringstirred overnight
- customThe phases were separated
- extractionthe water phase was extracted with methylene chloride
- washwashed with water and saturated salt solution
- dry with materialdried (MgSO4)
- customto give an oil
- customto give a mush, which
- customwas triturated with pentane
출처 및 근거
- ORD 기록
- ord-a7d939efcb5046068f80b05f6afc6d68
- 출처 데이터셋
- uspto-grants-1977_04
- 특허 번호
- US04020061
연결된 노트
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