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HRID 18768作成日:2026年10月26日

4-(Trifluoromethoxy)benzyl Chloride → 2-[(4-Trifluoromethoxybenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride

https://huagongshe.com/reaction/18768

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Trifluoromethoxy)benzyl ChlorideHCID 2777261—
反応物cis-4,5-Diphenylimidazolidine-2-thioneHCID 45258634—
溶媒EthanolHCID 702—
生成物2-[(4-Trifluoromethoxybenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole HydrochlorideHCID 6856948162.7%

反応手順

A mixture of intermediate 25 (200 mg, 0.786 mmol) and 4-trifluoromethoxybenzyl chloride (0.331 mg, 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 229 mg of the product 216. 1H NMR (DMSO-d6) δ 11.30 (s, 2 H), 7.75 (d, 2 H), 7.45 (d, 2 H), 7.20-6.90 (m, 6 H), 6.90-6.60 (m, 4 H), 5.79 (s, 2 H), 4.85 (s, 2 H); MS: m/z 429 (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-a0a374ffb69f439dae1ccb8425254a3c
出典メモuspto-grants-2010_06