Preparation method of 2, 2'-azino-bis(3-alkylbenzothiazoline-6-sulfonic acid) salt
A technology of alkylbenzene and thiazoline, which is applied in the field of preparation of 2,2′-azino-double salts, can solve the problems of high preparation cost, difficulty in procurement, and limited synthetic routes, and achieve high reaction yield, promote Development, easily accessible effects
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Embodiment 1
[0035] This example provides a preparation and purification process of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diamine salt (ABTS):
[0036] step 1:
[0037]
[0038] In a reactor, compound 2 was prepared by reacting 1 mole of compound 1 with diethyl sulfate. Wherein, the molar ratio of compound 1 to diethyl sulfate is 1:1; the solvent is tetrahydrofuran, the reaction temperature is 20° C., the reaction pressure is normal pressure, the reaction time is 8 hours, and the reaction is completed.
[0039] The solvent was spun off, ethyl acetate was added, washed twice with water, dried over anhydrous sodium sulfate, and then the ethyl acetate was spun off to obtain compound 2 with a yield of 65%.
[0040] Step 2:
[0041]
[0042] Compound 3 was prepared by reacting 1 mole of compound 2 with carbon disulfide in a reactor. Among them, the molar ratio of compound 2 to carbon disulfide is 1:1; the solvent is tetrahydrofuran, the reaction temperature is 60° C., ...
Embodiment 2
[0063] This example provides a preparation and purification process of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diamine salt (ABTS):
[0064] step 1:
[0065]
[0066] Compound 2 was prepared by reacting 1 mole of compound 1 with ethyl bromide in a reactor. Wherein, the molar ratio of compound 1 to bromoethane is 1:1; the solvent is tetrahydrofuran, the reaction temperature is 20° C., the reaction pressure is normal pressure, the reaction time is 8 hours, and the reaction is completed.
[0067] The solvent was spun off, ethyl acetate was added, washed twice with water, dried over anhydrous sodium sulfate, and then the ethyl acetate was spun off to obtain compound 2 with a yield of 60%.
[0068] Step 2:
[0069]
[0070] In a reactor, compound 3 is prepared by reacting 1 mole of compound 2, a halogenating agent (bromine) and carbon disulfide. Wherein, the molar ratio of compound 2 to the halogenation reagent is 1:1, the molar ratio of compound 2 to carbon...
Embodiment 3
[0091] This example provides a preparation and purification process of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diamine salt (ABTS):
[0092] step 1:
[0093]
[0094] Compound 2 was prepared by reacting 1 mole of compound 1 with ethyl bromide in a reactor. Wherein, the molar ratio of compound 1 to bromoethane is 1:1; the solvent is tetrahydrofuran, the reaction temperature is 20° C., the reaction pressure is normal pressure, the reaction time is 8 hours, and the reaction is completed.
[0095] The solvent was spun off, ethyl acetate was added, washed twice with water, dried over anhydrous sodium sulfate, and then the ethyl acetate was spun off to obtain compound 2 with a yield of 62%.
[0096] Step 2:
[0097]
[0098] In a reactor, compound 3 is prepared by reacting 1 mole of compound 2, a halogenating agent (bromine) and carbon disulfide. Wherein, the molar ratio of compound 2 to the halogenation reagent is 1:1, the molar ratio of compound 2 to carbon...
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