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ChemicalBook CAS DataBase List 1-Bromo-3,4,5-trimethoxybenzene
2675-79-8

1-Bromo-3,4,5-trimethoxybenzene synthesis

11synthesis methods
38790-07-7 Synthesis
1,2-Benzenediol, 5-bromo-3-methoxy-

38790-07-7
12 suppliers
inquiry

616-38-6 Synthesis
Dimethyl carbonate

616-38-6
675 suppliers
$5.00/5G

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Yield:2675-79-8 1256 g

Reaction Conditions:

with 1,8-diazabicyclo[5.4.0]undec-7-ene at 90;Large scale;Reagent/catalyst;

Steps:

1.3; 2.3; 3.3; 4.3; 5.3; 6.3 Synthesis of S3, 5-bromo-1,2,3-trimethoxybenzene (1)

Dissolve 1256 grams of Y-3 in 5.0 liters of dimethyl carbonate,1745 grams of DBU was added to the system, the system was naturally heated to 8-10 degrees, the oil bath was heated to 90 degrees and refluxed overnight, and the reaction was monitored by TLC until the reaction was complete. The reaction system was cooled to room temperature, and the reaction solution was concentrated to recover dimethyl carbonate. The concentrated reaction solution was poured into 5 liters of ethyl acetate and 2 liters of water. After stirring for 30 minutes, the layers were separated. The water layer was to be treated and the organic layer was used 1 liter in turn Wash twice with 2N HCl, twice with 1L 2N NaOH, and once with 1L water, and set aside the organic layer. The aqueous layer of the reaction solution, the acid aqueous layer, the alkaline aqueous layer, and the water-washed layer were extracted twice with 1 liter of ethyl acetate. The organic layers were combined, washed with 1L of saturated brine, dried with anhydrous sodium sulfate, and decolorized by adding activated carbon. It was filtered and spin-dried to obtain 1256 grams of crude product, which was recrystallized with ethanol-petroleum ether mixed solvent to obtain the pure product of target 1.

References:

CN113563163,2021,A Location in patent:Paragraph 0038; 0043-0054

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