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HRID 918756作成日:2026年10月26日

Iodine → 1-(4-chlorophenyl)-3-[(Z)-3-iodobut-2-enoxy]pyrazole

https://huagongshe.com/reaction/918756

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物1-(4-Chloro-phenyl)-3-((Z)-3-tributylstannanyl-but-2-enyloxy)-1H-pyrazoleHCID 131734873—
溶媒DichloromethaneHCID 6344—
生成物1-(4-chlorophenyl)-3-[(Z)-3-iodobut-2-enoxy]pyrazoleHCID 89650382—

反応手順

To 10.0 g (18.6 mmol) 1-(4-chloro-phenyl)-3-((Z)-3-tributylstannanyl-but-2-enyloxy)-1H-pyrazole in 100 ml methylene chloride have been added 4.7 g (18.6 mmol) iodine at ambient temperature with stirring which was continued for 3 h. After removal of the solvents in vacuo the crude product was dissolved in 200 ml MTBE. 100 ml 20% aqueous potassium fluoride solution have been added and the mixture was stirred for 2 h at ambient temperature. The aqueous layer was separated and extracted with 20 ml methyl-tert.-butyl ether twice. The combined organic phases have been washed twice with 20 ml of water each, dried with sodium sulfate, and the solvents were removed in vacuo. The crude product (7.2 g) has been purified by chromatography on 50 g silica with methyl-tert.-butylether/hexane (1:20). Yield 5.9 g, melting point 75-77° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09271501B2
出典データセットuspto-grants-2016_03
ORD IDord-d2ca9fdf88b74a30b3c38ffecb6e04e9
出典メモuspto-grants-2016_03