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HRID 329160作成日:2026年10月27日

1-Methylimidazole → 3-(2,4-dichlorophenoxy)-1-nitro-1-(tetrahydro-2H-1,3-thiazin-2-ylidene)-2-propanone

https://huagongshe.com/reaction/329160

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylimidazoleHCID 1390—
反応物2-nitromethylenetetrahydro-2H-1,3-thiazineHCID 42853—
反応物MAGNESIUM SILICATE (synthetic)HCID 61680—
反応物(2,4-Dichlorophenoxy)acetyl chlorideHCID 69887—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2,4-dichlorophenoxy)-1-nitro-1-(tetrahydro-2H-1,3-thiazin-2-ylidene)-2-propanoneHCID 86734697—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04020061
出典データセットuspto-grants-1977_04
ORD IDord-a7d939efcb5046068f80b05f6afc6d68
出典メモuspto-grants-1977_04