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HRID 70296作成日:2026年10月23日

Aminoacetaldehyde dimethyl acetal → 1-(3-bromophenyl)-1,3-dihydro-2H-imidazol-2-one

https://huagongshe.com/ja/reaction/70296

反応式

関与物質

役割名称HCID仕込み量
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
反応物3-Bromophenyl isocyanateHCID 141001—
溶媒DichloromethaneHCID 6344—
生成物1-(3-bromophenyl)-1,3-dihydro-2H-imidazol-2-oneHCID 44630681—

反応手順

A solution of 1-bromo-3-isocyanatobenzene (1.0 mL, 8.01 mmol) and [2,2-bis(methyloxy)ethyl]amine (0.86 mL, 8.01 mmol) in CH2Cl2 (15 mL) was stirred at room temperature for 16 hr. The solution was concentrated in vacuo and the residue taken up in a mixture of CH3CN (10 mL) and H2O (3 mL). TFA (3 mL) was added and the solution stirred at room temperature for 4 hr. The solution was concentrated in vacuo, the residue taken up in EtOAc then washed with satd NaHCO3, H2O, and brine. The organics were then dried over Na2SO4, concentrated in vacuo and the residue recrystallized from EtOAc to give 1-(3-bromophenyl)-1,3-dihydro-2H-imidazol-2-one as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 6.60 (d, J=3.0 Hz, 1H), 7.03 (d, J=3.0 Hz, 1H), 7.34-7.36 (m, 2H); 7.70-7.72 (m, 1H), 8.06 (s, 1H), 10.39 (br s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822518B2
出典データセットuspto-grants-2014_09
ORD IDord-49cfa41c1b5744d8b42a6de6d0d382f0
出典メモuspto-grants-2014_09