Fingerprint fluorescence fumigation developing reagent and developing method thereof
A fluorescent agent and fluorescence technology, applied in fluorescence/phosphorescence, material analysis through optical means, sensors, etc., can solve the problem of slow progress in the improvement of "502" glue fumigation and display technology, and little improvement in the properties of "502" glue, etc. question
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Embodiment 1
[0066] [Example 1] Preparation of 1-chloro-6-ethoxy-1,2,4,5-tetrazine (method 1):
[0067] Add dichloro-s-tetrazine (1 g, 6.66 mmol) into absolute ethanol (4.68 ml, 79.92 mmol), stir at room temperature for 0.5 h, dichloro-tetrazine dissolves, and continue stirring for 1.5 h. Extracted with ethyl acetate and water, dried over anhydrous sodium sulfate, separated and purified to obtain 781 mg of the target compound.
Embodiment 2
[0068] [Example 2] Preparation of 1-chloro-6-ethoxy-1,2,4,5-tetrazine (method 2):
[0069] Add dichloro-s-tetrazine (1 g, 6.66 mmol) into absolute ethanol (4.68 ml, 79.92 mmol), stir at room temperature for 0.5 h, dichloro-tetrazine dissolves, and continue stirring for 1.5 h. After adding 30ml of water, a red solid precipitated out, filtered it with suction, replaced solvent oil with acetonitrile and pumped it dry, and repeated twice to obtain 608 mg of the target compound. 1H NMR (400 MHz, Chloroform-d) δ 4.75 (q, J=7.1 Hz, 2H), 1.60 (t, J=7.1 Hz, 3H). LCMS: m / z=161(M+H)+
Embodiment 3
[0070] [Example 3] Preparation of 1-chloro-6-(2-fluoroethoxy)-1,2,4,5-tetrazine:
[0071] Add dichloro-s-tetrazine (500mg, 3.33mmol) into 5ml of dichloromethane, add 0.2ml of 2-fluoroethanol and 0.39ml of 2,6-lutidine at room temperature, stir at room temperature for 2h, extract with dichloromethane and water , dried over anhydrous sodium sulfate, separated and purified to obtain 318 mg of the target compound. 1H NMR (400MHz, Chloroform-d) δ 4.82 (m, 2H), 4.76 (m, 2H). LCMS: m / z=179(M+H)+
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