Synthesis method of benzocaprolactam
A technology of benzocaprolactam and synthesis method, which is applied in the direction of organic chemistry, can solve the problems of dangerous materials, use, and high cost, and achieve the effects of low cost, simple post-processing operation, and high output
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Embodiment 1
[0029] A kind of synthetic method of benzocaprolactam of the present invention comprises the following steps:
[0030] S1, using o-nitrotoluene as raw material, condensing reaction with acrylate under alkali catalysis to obtain o-nitrobenzene butyric acid or its ester;
[0031] S2. O-nitrophenylbutyric acid or its ester reduces the nitro group and closes the ring to obtain the target product. The reaction principle of the present invention is as figure 1 shown.
[0032] The concrete implementation mode of the present invention is:
[0033] Preparation of methyl o-nitrobenzenebutyrate: put 500 g of o-nitrotoluene, 20 g of methyl acrylate, and 1 g of a phase transfer catalyst (such as tetrabutylammonium bromide) into a four-necked flask; heat up to 35° C., and slowly add hydrogen dropwise Concentrated potassium hydroxide aqueous solution prepared with 13 g of potassium oxide; react for 1 hour after the dropwise addition, add 200 g of water, and separate layers to obtain an aq...
Embodiment 2
[0037] The concrete implementation mode of the present invention is:
[0038] Preparation of methyl o-nitrobenzenebutyrate: put 3000 g of o-nitrotoluene, 200 g of methyl acrylate, and 10 g of a phase transfer catalyst (such as tetrabutylammonium bromide) into a four-necked flask; heat up to 35 ° C, slowly dropwise add hydrogen to oxidize Concentrated potassium hydroxide aqueous solution prepared with 130g of potassium; after the dropwise addition, react for 1 hour, add dilute sulfuric acid to adjust the pH to 1; add 1000g of dichloromethane for extraction three times; combine dichloromethane, dry over sodium sulfate, concentrate to remove solvent, and vacuum distill In addition to o-nitrotoluene, the black oil obtained was methyl o-nitrobenzene butyrate, with a yield of 77% and a purity of 68% by HPLC; 1H NMR (400MHz, DMSO) δ1.90-1.97 (m, 2H), 2.32– 2.36(m,2H),2.84–2.88(m,2H),3.61(s,3H),7.29–7.32(m,2H),7.45–7.49(m,1H),7.81–7.83(d,1H);
[0039] Preparation of benzocaprolactam:...
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