Process for synthesizing o-chloro-anisole
A synthesis method and a technology for chloroanisole are applied in the field of synthesis of fine chemical intermediates, can solve the problems of high price, environmental pollution, difficult recycling and the like, and achieve good industrial application prospects, low environmental pollution, and product yield. high effect
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Embodiment 1
[0020] In the reactor, o-dichlorobenzene (44.1g, 0.3mol), sodium methoxide solution (115.7g, 0.6mol) and N,N-dimethylformamide (100ml) with a mass fraction of 28% were mixed, while adding CuBr (3g, 0.021mol) was used as a catalyst, and the methanol was distilled under stirring until the kettle temperature reached 135°C and then refluxed for 20 hours; (30ml×3) extraction, and rectification of the organic liquid to obtain 32.2g of the compound o-chloroanisole, with a yield of 75.6%.
[0021] The experimental data are as follows:
[0022] b.p.193-195°C; 1 HNMR (400MHz, CDCl 3 )δ (ppm): 3.82 (s, 3H, OCH 3 ), 6.80-7.17 (m, 4H, ArH); IR (liquid film) cm -1 : 3057, 2999, 2965, 2940, 1583, 1549, 1462, 1300, 1253, 1134, 1026, 941; CI-MS: 142 (M + )
Embodiment 2
[0024] In the reactor, o-dichlorobenzene (58.8g, 0.4mol), a mass fraction of 28% sodium methoxide solution (38.6g, 0.2mol) and N,N-dimethylformamide (100ml) were mixed, and added CuBr (3g, 0.021mol) was used as a catalyst; the methanol was distilled under stirring until the temperature of the kettle reached 135°C and then refluxed for 20 hours; (30ml×3) extraction, and distillation of the organic liquid to obtain 8.1 g of the compound o-chloroanisole, with a yield of 28.5%.
Embodiment 3
[0026] According to the method in Example 1, the feeding amount of the sodium methoxide solution was 231.4 g, and 32.4 g of o-chloroanisole was obtained after the reaction, with a yield of 76.1%.
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