Preparation method and application of C23-38 cycloaliphatic diisocyanate
A technology of diisocyanate and cycloaliphatic diisocyanate, which is applied in the field of preparation of C23-38 cycloaliphatic diisocyanate, can solve the problems of easy yellowing of materials, high production difficulty, and small molecular weight of IPDI, so as to facilitate industrial promotion, application and production Raw materials are easy to obtain and the production difficulty is small
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Embodiment 1
[0036] Example 1: Preparation C 23 Cycloaliphatic diisocyanate
[0037] Step 1: add 500g (1.7mol) dehydrated methyl ricinoleate, 146.2g (1.7mol) methyl acrylate, and inhibitor hydroquinone 1.5g in the 2000mL pressure reactor, and replace the air in the kettle with nitrogen, Heating to 160-180°C and reacting for 3.5 hours to obtain the crude dibasic acid methyl ester.
[0038] It should be noted that the reaction of dehydrated ricinoleic acid methyl ester and methyl acrylate in this embodiment can be replaced by the reaction of dehydrated ricinoleic acid and acrylic acid, and the dibasic acid methyl ester in the following steps can also be the corresponding binary Acids, in view of space, are not given one by one, and in this embodiment, only the reaction of dehydrated ricinoleic acid methyl ester and methyl acrylate is taken as an example.
[0039] Step 2: Add 380 g (1.0 mol) of the dibasic acid methyl ester generated in step 1 and 5 g of tributyl phosphate into a 1000 mL fo...
Embodiment 2
[0053] Example 2: Preparation C 24 Cycloaliphatic diisocyanate
[0054] The difference between this embodiment and Example 1 is that the raw materials for preparing cycloaliphatic diisocyanate are different, and the present embodiment uses 500g (1.7mol) dehydrated methyl ricinoleate and 170.0g (1.7mol) α-methyl methacrylate Reaction, preparation process is identical with embodiment 1, obtains target product C 24 Aliphatic diisocyanate, namely 1-hexyl-3'-methyl-3-(2-isocyanatoethyl)-4-(8-isocyanatooctyl)cyclohexane.
[0055] Molecular formula: C 24 h 42 N 2 o 2
[0056] Molecular weight: 390
[0057] Appearance: light yellow oily liquid
[0058] NCO content: 19.4-21.5%
[0059] Structural formula:
[0060]
[0061] The infrared spectrometry data are as follows:
[0062] IR(kBr)γ(cm -1 ):2853.7, 2924.4 (-CH 2 ,-CH 3 C-H stretching vibration);
[0063] 1463.81354.2 (C-CH 3 , C-H deformation vibration);
[0064] 723.0–(CH 2 ) 4 skeleton vibration;
[0065] 2...
Embodiment 3
[0066] Example 3: Preparation C 24 Cycloaliphatic diisocyanate
[0067] The difference between this embodiment and Example 1 is that the raw materials for preparing cycloaliphatic diisocyanate are different, and the present embodiment uses 500g (1.7mol) dehydrated methyl ricinoleate and 170.0g (1.7mol) β-methyl methacrylate Reaction, preparation process is identical with embodiment 1, obtains target product C 24 Aliphatic diisocyanate, namely 1-hexyl-2-methyl-3-(2-isocyanatoethyl)-4-(8-isocyanatooctyl)cyclohexane.
[0068] Molecular formula: C 24 h 42 N 2 o 2
[0069] Molecular weight: 390
[0070] Appearance: light yellow oily liquid
[0071] NCO content: 19.4-21.5%
[0072] Structural formula:
[0073]
[0074] The infrared spectrometry data are as follows:
[0075] IR(kBr)γ(cm -1 ):2853.7, 2924.4 (-CH 2 ,-CH 3 C-H stretching vibration);
[0076] 1463.81354.2 (C-CH 3 , C-H deformation vibration);
[0077] 723.0–(CH 2 ) 4 skeleton vibration;
[0078] 22...
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