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Chemical Structure| 20461-86-3 Chemical Structure| 20461-86-3

Structure of 20461-86-3

Chemical Structure| 20461-86-3

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Product Details of [ 20461-86-3 ]

CAS No. :20461-86-3
Formula : C6H12O4
M.W : 148.16
SMILES Code : O=C(O)C(OCC)OCC
MDL No. :MFCD06208355
InChI Key :WFVKIANRKSZMGB-UHFFFAOYSA-N
Pubchem ID :3017504

Safety of [ 20461-86-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H335-H314
Precautionary Statements:P260-P264-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P403+P233-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 20461-86-3 ]

* 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 [ 20461-86-3 ]

[ 20461-86-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 5344-23-0 ]
  • [ 20461-86-3 ]
  • [ 621-63-6 ]
  • 2
  • [ 621-63-6 ]
  • [ 20461-86-3 ]
  • 3
  • [ 5430-45-5 ]
  • [ 20461-86-3 ]
  • [ 31224-40-5 ]
YieldReaction ConditionsOperation in experiment
68% With ammonium peroxydisulfate; caesium carbonate; In dimethyl sulfoxide; at 20℃; for 24h;Inert atmosphere; Irradiation; Green chemistry; General procedure: Heterocycle (0.10mmol,1equiv)ammonium persulfate (0.30 mmol, 3 equiv), Cs2CO3(0.20mmol,2 equiv)were placed in a dry glass tube.Then, anhydrous DMSO1 mL) and2,2-diethoxyacetic acid (0.7mmol7equiv), wereinjected into the tube by syringe under a N2atmosphere.The solution was then stirred at roomtemperature under the irradiation of 15W blueLEDs strip for 24h.After completion of the reaction,the mixture was quenched by addition of1.2mL of 3.0 M HCl, stirred for 20hthen saturated Na2CO3solution was added to adjust pH tobasicextract with CH2Cl2,the combined organic layers was washed with brine, then dry overanhydrous Na2SO4. The desired products were obtained in thecorresponding yields afterpurification by flashchromatography on silica gel eluting with petroleum and ethylacetate.
68% At room temperature, will be 66 mg (0.4 mmol) 5 - chloroisonicotinic quinoline, 414 mg (2.8 mmol) 2, 2 - ethoxy acetic acid, 182 mg (0.8 mmol) of the ammonium persulfate and 260 mg (0.8 mmol) Cs2CO3Dissolved in 6 ml in dimethyl sulfoxide, mix, nitrogen 30 min after the blue LEDs arranged under the lamp illumination reaction 20 h, adding 7.2 concentration is 3 M hydrochloric acid catalytic hydrolysis 20 h, using sodium carbonate adjusting pH to neutral, extraction, the combined organic phase, by the rotary concentrate by the Rotavapor after turns on lathe does, then to the volume ratio of 15:1 petroleum ether: ethyl acetate mixed solution of eluant, performing silica gel column chromatography purification and separation, to obtain the corresponding formylation heterocyclic derivatives, its reaction is: Product purity is 99%, and the yield is 68%.
  • 4
  • [ 1632-83-3 ]
  • [ 20461-86-3 ]
  • [ 3012-80-4 ]
YieldReaction ConditionsOperation in experiment
40% With ammonium peroxydisulfate; caesium carbonate; In dimethyl sulfoxide; at 20℃; for 24h;Inert atmosphere; Irradiation; Green chemistry; General procedure: Heterocycle (0.10mmol,1equiv)ammonium persulfate (0.30 mmol, 3 equiv), Cs2CO3(0.20mmol,2 equiv)were placed in a dry glass tube.Then, anhydrous DMSO1 mL) and2,2-diethoxyacetic acid (0.7mmol7equiv), wereinjected into the tube by syringe under a N2atmosphere.The solution was then stirred at roomtemperature under the irradiation of 15W blueLEDs strip for 24h.After completion of the reaction,the mixture was quenched by addition of1.2mL of 3.0 M HCl, stirred for 20hthen saturated Na2CO3solution was added to adjust pH tobasicextract with CH2Cl2,the combined organic layers was washed with brine, then dry overanhydrous Na2SO4. The desired products were obtained in thecorresponding yields afterpurification by flashchromatography on silica gel eluting with petroleum and ethylacetate.
 

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