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Chemical Structure| 69630-16-6 Chemical Structure| 69630-16-6

Structure of 69630-16-6

Chemical Structure| 69630-16-6

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Product Details of [ 69630-16-6 ]

CAS No. :69630-16-6
Formula : C7H15N3O2
M.W : 173.21
SMILES Code : O=C(N1CCOCC1)NCCN
MDL No. :MFCD16301502

Safety of [ 69630-16-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 69630-16-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 69630-16-6 ]

[ 69630-16-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 154467-16-0 ]
  • [ 69630-16-6 ]
YieldReaction ConditionsOperation in experiment
99.5% With sodium sulfate; sodium hydroxide; In dichloromethane; at 30℃;Large scale; Add 30 kg of dichloromethane to the reaction kettle and after 3.0 kg of N-(2-aminoethyl)-4-morpholinecarboxamide oxalate, Add 5.0 kg of anhydrous sodium sulfate, Sodium hydroxide 1.14kg. The reaction was carried out at 30 C for 15-18 h. filter, the filtrate was concentrated to dryness under reduced pressure. Get about 1.97kg of light yellow oil, The yield was 99.5%.
84.67% With sodium hydroxide; In water; at 20 - 47℃; for 0.333333h;pH 10-11.5; At room temperature, 15.8 g of the compound represented by the formula III and 47.4 g of water were added to a 100 mL reaction flask, Stir, Heating to 43 ~ 47 deg C full solution, 40% sodium hydroxide solution was added dropwise with stirring, Adjust the pH to 10 ~ 11.5, Keep warm for about 20 minutes; Cooled to room temperature, filter, The filter cake was rinsed with 7.2 g of water, The filtrate into the rotary bottle, At a temperature of 44 to 48 C and a pressure of P ≤ -0.07 MPa, Concentrated to no distillate distillate, The remaining residue was reduced to room temperature, Adding 110 g of acetone, Stirring to the residue all dispersed in acetone ,And then transferred into a 250mL Erlenmeyer flask, 9.48 g of anhydrous sodium sulfate was dried for 3 hours, filter, The filtrate was transferred to an eggplant-shaped flask and concentrated by rotary evaporation until no fraction, To give pure intermediate of formula IV, A light yellow oil, 8.8 g, The yield was 84.67%.
 

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