Method for preparing dodecylphenol
A technology of dodecyl phenol and phenol is applied in the field of preparation of dodecyl phenol and organic compounds, which can solve the problems of low purity of alkyl phenol products, poor anti-oxidative stability, long reaction time, etc., and achieves improved utilization. Value, long service life, light effect of product color
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] In a three-necked flask reactor with an electric stirring device and a vacuum treatment device, in 45mL of petroleum ether (petroleum ether with a boiling range of 90-120°C), the amount of solvent used is 2.5 times the liquid volume of phenol, 0.2mol of phenol, 1.0mL of relative Boron trifluoride ether solution catalyst with a density of 1.12-1.14 is put into a three-necked flask, and the catalyst dosage is 12% of the mass of phenol. The molar ratio of polyisobutene is 2:1. After stirring and reacting for 2 hours at the reaction temperature of 20°C, the reaction mixture is suction-filtered while it is hot, and the filtrate is washed with hot water 5 times while it is hot to remove waste water. The crude product was distilled under reduced pressure, and the distillate product was obtained at a vacuum degree of 1.3 mb and a temperature of 150 ° C. Finally, under the protection of nitrogen, the reaction mixture was filtered while hot, and the filtrate was washed with hot wa...
Embodiment 2
[0022] The preparation method is the same as in Example 1, except that 0.2 mol of phenol and 3 g of cation exchange resin Amberlyst 15 catalyst are used instead of the corresponding raw materials in Example 1, the amount of catalyst used is 15% of the mass of phenol, the reaction environment is vacuum treated, and the reaction environment is vacuum-processed at a temperature of 50 ° C. After fully stirring and mixing evenly, add a total amount of 0.1mol trimeric isobutylene dropwise under continuous stirring, the molar ratio of phenol to trimeric isobutylene is 2:1, and at a reaction temperature of 50°C, stir and react for 6 hours, and then dissolve the reaction mixture while it is hot. Carry out suction filtration, product aftertreatment is with example 1.
Embodiment 3
[0024] The preparation method is the same as in Example 1, except that 0.2 mol of phenol and 3 g of strongly acidic aluminum silicate pellet molecular sieve catalyst are used instead of the corresponding raw materials in Example 1, the amount of catalyst used is 15% of the mass of phenol, the reaction environment is vacuum treated, and the reaction environment is vacuum-treated at 90° C. After fully stirring and mixing evenly at high temperature, add dropwise a total of 0.1 mol of trimeric isobutylene under continuous stirring, the molar ratio of phenol to trimeric isobutylene is 2:1, and at a reaction temperature of 90°C, after stirring for 10 hours, The reaction mixture was suction filtered while hot. Product post-processing is the same as Example 1.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com