2-Chloro-1H-imidazole synthesis
- Product Name:2-Chloro-1H-imidazole
- CAS Number:16265-04-6
- Molecular formula:C3H3ClN2
- Molecular Weight:102.52
61278-81-7
16265-04-6
The general procedure for the synthesis of 2-chloroimidazole from 1-(diethoxymethyl)imidazole is as follows: with reference to Example 9, 2-chloroimidazole was prepared as follows: N-(diethoxymethyl)imidazole (50.0 g) was dissolved in tetrahydrofuran (200 ml), and a n-hexane solution of 2.6 M n-butyllithium (120 ml) was added slowly and dropwise to this solution. The addition of tetrahydrofuran solution (100 ml) of hexachloroethane (73.9 g) was continued dropwise at -35°C. The reaction mixture was kept at the same temperature for 5 min, then warmed up to -20°C and 6N hydrochloric acid (100 ml) was added, after which it was restored to room temperature and left to stand for 5 min. The aqueous layer was separated and the organic layer was extracted with 1N hydrochloric acid, the extract was combined with the aqueous layer and washed with ether. This was followed by neutralization with 6N aqueous sodium hydroxide and extraction with ethyl acetate. The organic layer was separated, dried with anhydrous magnesium sulfate and the solvent was removed by distillation to give the crude product. The crude product was ground with dichloromethane to give finally 2-chloroimidazole (26.0 g, yield: 85.0%) as a light brown solid.1H-NMR (CDCl3) δ (ppm): 10.64 (1H, bs), 7.05 (1H, s).
61278-81-7
44 suppliers
$272.00/10ml
16265-04-6
154 suppliers
$14.00/100mg
Yield:16265-04-6 85%
Reaction Conditions:
Stage #1: 1-(diethoxymethyl)-1H-imidazolewith n-butyllithium in tetrahydrofuran;hexane at -35;
Stage #2: with hexachloroethane in tetrahydrofuran;hexane at -35; for 0.0833333 h;
Stage #3: with hydrogenchloride;sodium hydroxidemore than 3 stages;
Steps:
9 Preparation of 2-chloroimidazole
Reference example 9 Preparation of 2-chloroimidazole N-(Diethoxymethyl)imidazole (50.0 g) was dissolved in tetrahydrofuran (200 ml), to this solution was added dropwise n-hexane solution (120 ml) of 2.6M n-butyllithium at lower than -35°C, next tetrahyfrofuran solution (100 ml) of hexachloroethane (73.9 g) was added dropwise. Reaction mixture was allowed to stand at the same temperature for 5 minutes, then temperature was rised, after being added 6N hydrochloric acid (100 ml) at -20°C, then turned back to room temperature, and allowed to stand for 5 minutes. The aqueous layer was taken by separation, and the organic layer was extracted with 1N hydrochloric acid, the extract was combined with the former aqueous layer, and washed with diethyl ether, then neutralized with an aqueous solution of 6N sodium hydroxide, and extracted with ethyl acetate. The organic layer was taken by separation, after being dried over anhydrous magnesium sulfate, the solvent was removed by distillation to obtained a crude product. This crude product was triturated with methylene chloride, there was obtained 2-chloroimidazole (26.0 g, yield: 85.0%) as pale brown solid product. 1H-NMR (CDCl3) δ (ppm): 10.64 (1H, bs), 7.05 (1H, s).
References:
EP1553088,2005,A1 Location in patent:Page/Page column 52
15469-97-3
216 suppliers
$9.00/250mg
16265-04-6
154 suppliers
$14.00/100mg
288-32-4
1029 suppliers
$5.00/25g
16265-04-6
154 suppliers
$14.00/100mg