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HRID 842128作成日:2026年10月27日

Propargyl alcohol → 5-Chloro-2-(2-chlorophenyl)-7-(3-hydroxy-1-propynyl)-benzoxazole

https://huagongshe.com/reaction/842128

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl alcoholHCID 7859—
反応物7-Bromo-5-chloro-2-(2-chlorophenyl)-1,3-benzoxazoleHCID 4639254—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒TolueneHCID 1140—
溶媒TriethylamineHCID 8471—
生成物5-Chloro-2-(2-chlorophenyl)-7-(3-hydroxy-1-propynyl)-benzoxazoleHCID 2261828185.8%

反応手順

A solution of 17.15 g (50 mmol) of 7-bromo-5-chloro-2-(2-chlorophenyl)-benzoxazole and 4.40 ml (75 mmol) of propargylalcohol in 32 ml of toluene and 64 ml of triethylamine was heated under nitrogen to 80-5° C. with 175.4 mg (250 μM) of bis(triphenylphosphine)palladium (II) chloride and 8.6 mg (4.5 μM) of copper (1) iodide. After 6 hours, the solid was filtered off and washed with dichloromethane. The solution was evaporated in vacuo. The residue was dissolved in ethyl acetate, washed with 1 N HCl, sodium bicarbonate solution, and water. The ethyl acetate was removed in vacuo, the residue (15.46 g) was dissolved in dichloromethane and filtered through 60 g of silica gel to give the title compound (13.64 g, 85.8%), mp 165-9° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06372770B1
出典データセットuspto-grants-2002_04
ORD IDord-aee9e3d6108e4747bb00479c6329acf7
出典メモuspto-grants-2002_04