Method for synthesizing oxazoline derivative by use of amide
A technology for synthesizing oxazoline and derivatives, applied in the direction of organic chemistry and the like, can solve the problems of high risk and low yield, and achieve the effects of low toxicity, low price and cost reduction
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Embodiment 1
[0021] 121g of benzamide, 56g of 2-butene, 256g of I 2 and 322g PhI(OAc) 2 The catalyst combination was added to 500mL of chloroform, stirred at 30°C, irradiated with a high-pressure mercury lamp for 6 hours, washed with water, and the organic phase was separated and dried, and the organic phase was distilled off under reduced pressure to obtain a solid, namely The oxazoline derivative with the structure shown in formula (III) has a product yield of 92%.
[0022]
Embodiment 2
[0024] 135g of p-toluamide, 56g of 2-butene, 256g of I 2 and 322g PhI(OAc) 2 The catalyst combination was added into 500mL of chloroform, stirred at 40°C, irradiated with a high-pressure mercury lamp for 6 hours, washed with water, and the organic phase was separated and dried, and the organic phase was distilled off under reduced pressure to obtain a solid, namely The oxazoline derivative with the structure shown in formula (III) has a product yield of 91%.
[0025]
Embodiment 3
[0027] 135g of p-toluamide, 69g of 2-pentene, 256g of I 2 and 322g PhI(OAc) 2 The catalyst combination was added into 500mL of chloroform, stirred at 40°C, irradiated with a high-pressure mercury lamp for 6 hours, washed with water, and the organic phase was separated and dried, and the organic phase was distilled off under reduced pressure to obtain a solid, namely The oxazoline derivative with the structure shown in formula (III) has a product yield of 91%.
[0028]
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