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HRID 22263作成日:2026年10月23日

Ammonium Chloride → 1-(Diphenylmethyl)-4-[(2-phenyl-4-methylfuran-5-yl)eth-1-yl]piperazine

https://huagongshe.com/ja/reaction/22263

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物BenzhydrylpiperazineHCID 70048—
反応物Sodium BicarbonateHCID 516892—
反応物2-Phenyl-4-methyl-5-formylfuranHCID 19430267—
反応物HCID 178418373HCID 178418373—
触媒Titanium isopropoxideHCID 11026—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物1-(Diphenylmethyl)-4-[(2-phenyl-4-methylfuran-5-yl)eth-1-yl]piperazineHCID 54216582—

反応手順

A solution of 2-phenyl-4-methyl-5-formylfuran (1.1 g), diphenylmethylpiperazine (1.5 g), and titanium(IV) isopropoxide (1.76 g) was stirred for 11/4 hours. Diethyl ether (20 ml) was added, and the resultant solution was stirred for 30 minutes. Methyl magnesium iodide (6 ml of 3M in ether) was then added dropwise, and the mixture stirred at room temperature for 1 hour. Ammonium chloride (20 ml of a saturated solution in water) was then added, followed by 300 ml of methylene chloride, and the mixture made basic with a solution of sodium bicarbonate. The residue was partitioned between methylene chloride/water, the organic layer separated, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was flash-chromatographed on silica gel, eluting with 15% ethyl acetate in heptane with a trace of ammonia, to yield 0.51 g of 1-(diphenylmethyl)-4-[(2-phenyl-4-methylfuran-5-yl)eth-1-yl]piperazine. Treatment with anhydrous hydrochloric acid in ethanol converted the base to its dihydrochloride salt, m.p. 205°-208° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428037
出典データセットuspto-grants-1995_06
ORD IDord-9c8de45512cf42c6925872739c3f6448
出典メモuspto-grants-1995_06