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HRID 2053572作成日:2026年10月26日

p-Trifluoromethylbenzyl chloride → 2-[(4-Trifluoromethylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride

https://huagongshe.com/reaction/2053572

反応式

関与物質

役割名称HCID仕込み量
反応物p-Trifluoromethylbenzyl chlorideHCID 123096—
反応物cis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
溶媒EthanolHCID 702—
生成物2-[(4-Trifluoromethylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856845874.3%

反応手順

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 4-trifluoromethylbenzyl chloride (0.232 mL, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 262 mg of the product 228. 1H NMR (DMSO-d6) δ 11.42 (s, 2H), 7.95-7.90 (m, 4H), 7.15-6.90 (m, 6H), 6.90-6.65 (m, 4H), 5.77 (s, 2H), 4.92 (s, 2H); MS: m/z 413 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07326792B2
出典データセットuspto-grants-2008_02
ORD IDord-ea16030f43244e1f97670625678ab004
出典メモuspto-grants-2008_02