Synthesis method of compound 1-(2-halogenophenyl)-3-methyl-butanone-1
A synthetic method, the technology of halophenyl, applied in the field of organic chemical synthesis, can solve the problems of non-compliance with green chemistry requirements, many side reactions, and inapplicability, and achieve the effects of low cost, high product quality, and few side reactions
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Embodiment 1
[0020] Embodiment 1, the synthesis of 1-(2-chlorophenyl)-3-methyl-butanone-1
[0021] (1) Synthesis of 2-chloro-N-methoxy-N-methylbenzamide
[0022] In a round bottom flask, add 2-chlorobenzoic acid (15.65g, 0.1 mol), N-methoxymethylamine (18.3g, 0.3 mol), anhydrous toluene (200ml), cool to about 0°C in an ice bath, Add the toluene solution of phosphorus trichloride (phosphorus trichloride 6.878g, 0.05 mol, toluene 100 ml) dropwise, stir for 30 minutes, then warm up to room temperature, react for 2 hours, then heat up to about 60°C, continue to react for 30 minutes ; After the reaction, add saturated NaHCO to the reaction mixture 3 The solution was quenched, extracted with ethyl acetate (3 × 200 mL), the organic phases were combined, MgSO 4 Dry, filter, concentrate, and purify by column chromatography to obtain 2-chloro-N-methoxy-N-methylbenzamide. 19.5 g, yield 97.7%.
[0023] 1 HNMR (400 MHz, CDCl 3 ): δ (ppm): 7.42~7.28 (m, 4H), 3.47 (s, 3H), 3.39 (s, 3H).
[0024] (...
Embodiment 2
[0028] Embodiment two, the synthesis of 1-(2-fluorophenyl)-3-methyl-butanone-1
[0029] (1) Synthesis of 2-fluoro-N-methoxy-N-methylbenzamide
[0030] In a round bottom flask, add 2-fluorobenzoic acid (163.6g, 1mol), N-methoxymethylamine (183g, 3mol), anhydrous toluene (600ml), cool to about 0°C in an ice bath; Add the toluene solution of phosphorus trichloride dropwise (phosphorus trichloride 0.5mol, toluene 100 ml), react for 30 minutes, then raise the temperature to room temperature and react for 2 hours, then raise the temperature to 60 o C for 30 minutes; after the reaction, add saturated NaHCO 3 The solution was quenched, extracted with ethyl acetate (3 x 5 mL), the organic phases were combined, MgSO 4 Dry, filter, concentrate, and purify by column chromatography to obtain 2-fluoro-N-methoxy-N-methylbenzamide. 211.48g, yield 98.9%.
[0031] 1 HNMR (400 MHz, CDCl 3 ): δ (ppm): 7.45~7.39 (m, 2H), 7.38~7.19 (m, 1H), 7.18~7.08 (m, 1H), 3.53 (S, 3H), 3.35 (S, 3H); 13 C...
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