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HRID 18754作成日:2026年10月23日

3-(Trifluoromethyl)benzyl chloride → 2-[(3-Trifluoromethylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride

https://huagongshe.com/ja/reaction/18754

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)benzyl chlorideHCID 69716—
反応物cis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
溶媒EthanolHCID 702—
生成物2-[(3-Trifluoromethylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856713355.5%

反応手順

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 3-trifluoromethylbenzyl chloride (0.243 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 196 mg of the product 202. 1H NMR (DMSO-d6) δ 11.32 (s, 2 H), 8.10-7.65 (m, 4 H), 7.15-6.95 (m, 6 H), 6.90-6.60 (m, 4 H), 5.78 (s, 2 H), 4.93 (s, 2 H); MS: m/z 413 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741493B2
出典データセットuspto-grants-2010_06
ORD IDord-e67f4e8fc0d9441fbf3b9cfecc6b4d92
出典メモuspto-grants-2010_06