Synthesis method of 1-chloromethyl naphthalene and application of catalyst and non-cationic surfactant thereof
A technology of surfactant and chloromethyl naphthalene, which is applied in the field of non-cationic surfactants, can solve the problems of low reaction yield and long reaction time, and achieve the effects of high yield and content, easy operation, and reduction of three wastes
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[0042] A kind of synthetic method of 1-chloromethylnaphthalene, the method uses the catalyst that the synthetic 1-chloromethylnaphthalene proposed by the present invention is used, and the method comprises the following steps:
[0043]a), formaldehyde or paraformaldehyde and naphthalene, concentrated hydrochloric acid, catalyzer are mixed, and catalyzer is the catalyzer that the synthetic 1-chloromethylnaphthalene of the present invention proposes, and the mass ratio of catalyzer and naphthalene is 0.01~0.04: 1, naphthalene and The molar ratio of concentrated hydrochloric acid is 1:1.8~3, and the molar ratio of naphthalene to formaldehyde or paraformaldehyde is 1:1.5~2.5; there is no order in adding the two components of the catalyst;
[0044] b), stirring and reacting at the reaction temperature for a period of time, the reaction temperature is 70-90°C, the reaction temperature is preferably 75-80°C, and the reaction period is 3-5 hours;
[0045] c), cooled to room temperatur...
Embodiment 1
[0053] In a 500ml three-necked flask equipped with a thermometer and a condenser tube, add 25.6g (0.20mol) of naphthalene, 11g (converted into formaldehyde 0.37mol) of paraformaldehyde, and 40ml of 36% concentrated hydrochloric acid (0.47mol) respectively. The weight ratio of the catalyst is 1.000:0.03, and the composition of the catalyst is tetraethylammonium bromide:N, N-sodium oleoylmethyl taurate=1:0.5. Stir at 75°C for 5h. After cooling, extract with cyclohexane and use 10% NaHCO 3 The solution was washed, and the cyclohexane was removed by rotary evaporation. Carried out vacuum distillation to obtain 33.86 g of 99.1% 1-chloromethylnaphthalene product. The product yield of 1-chloromethylnaphthalene is 95.7%.
Embodiment 2
[0058] In a 500ml three-neck flask equipped with a thermometer and a condenser tube, add 12.8g (0.10mol) of naphthalene, 6g (converted into formaldehyde 0.20mol) of paraformaldehyde, and 18ml of concentrated hydrochloric acid (0.21mol), according to the weight ratio of naphthalene to catalyst The catalyst is added at a ratio of 1.000:0.04, and the composition of the catalyst is tetraethylammonium chloride: fatty acid diethanolamide=1:0.2. Stir at 80°C for 4h. After cooling, extract with cyclohexane and use 10% NaHCO 3 The solution was washed, and the cyclohexane was removed by rotary evaporation. Carried out vacuum distillation to obtain 16.84 g of 99.3% 1-chloromethylnaphthalene product. The product yield of 1-chloromethylnaphthalene is 95.4%.
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