A simple and controllable method for synthesizing α-mercapto-ω-hydroxyl polyethers using thiocarboxylic acid as an initiator
A technology of thiocarboxylic acid and hydroxyl polyether, which is applied in the field of polyether synthesis, can solve problems such as the slow development of synthesis methods, and achieve the effect of a wide range of sources
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Embodiment 1
[0052] One-pot two-step synthesis of α-mercapto-ω-hydroxypolyethylene oxide. (1) Ring-opening polymerization of ethylene oxide (EO) was carried out using thioacetic acid as an initiator and a metal-free Lewis acid-base pair as a catalyst; (2) In situ aminolysis deacetylation. The specific operation is as follows:
[0053] Both tetrahydrofuran (THF) and EO are used after purification and dehydration treatment, and thioacetic acid can be used directly. Under an inert atmosphere, mix 1 part of thioacetic acid (0.5 mmol), 0.1 part of phosphazene base t BuP 1 , 0.5 parts of tri-sec-butylborane and THF (1ml) were successively added into a dry glass reactor and stirred and mixed evenly. In this example, the molar ratio of thioacetic acid, organic base and alkylboron was 1:0.1:0.5 . Connect the glass reactor to a vacuum line, remove part of the gas in the bottle, and cool down with an ice-water bath. Distilled 90 parts of dry EO (where [EO] 0 =15mol / L), and react in a sealed gla...
Embodiment 2
[0056]Two-pot synthesis of α-mercapto-ω-hydroxypolyethylene oxide. (1) With thioacetic acid as initiator, metal-free Lewis acid-base pair is the ring-opening polymerization of ethylene oxide (EO) implemented as a catalyst; (2) the α-thioacetate-ω obtained in the first step After the -hydroxypolyethylene oxide precipitate is dried, the acetyl group is deacetylated by ammonia cleavage. The specific operation is as follows:
[0057] The first step epoxy polymerization is with embodiment 1. After the end of the polymerization reaction, the product was collected, diluted with THF (2mL) and added with neutral Al 2 o 3 Stir, filter twice, and vacuum dry to obtain α-thioacetate-ω-hydroxypolyethylene oxide. Under an inert atmosphere, weigh the initial product in a clean glass reactor, add 7.0 mol / L ammonia in methanol solution (the amount of ammonia used is 10 parts) and methanol (1 mL), and react at room temperature for 8 h. After the reaction was completed, the vacuum line was c...
Embodiment 3
[0059] Change the amount of Lewis acid-base pair, add 0.01 part of phosphazene base t BuP 1 And 0.01 part of tri-sec-butylborane, the rest are consistent with Example 1, and the EO polymerization time is extended to 6h. In this example, the molar ratio of thioacetic acid, organic base and alkyl boron is 1:0.01:0.01. After the first polymerization reaction is completed, 1 The conversion rate of EO monomer was 100% as measured by H NMR, the molecular weight of the crude product as measured by SEC was 4.3 kg / mol, and the degree of dispersion was 1.10. 1 H NMR (600MHz, Chloroform-d), δ3.92 (ddd, J=9.1, 6.3, 2.8Hz, 2H), 3.65 (m, 366H), 3.02 (dq, J=5.1, 1.8Hz, 2H), 2.34 (d,J=1.3Hz,3H).
[0060] After the second step ammonolysis reaction finishes, 1 The degree of thiol functionalization as measured by H NMR is 100%, the molecular weight of the product as measured by SEC is 4.2 kg / mol, and the degree of dispersion is 1.09. 1 H NMR (600MHz, Chloroform-d), δ3.93 (d, J=6.4Hz, 2H), ...
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