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Chemical Structure| 78315-99-8 Chemical Structure| 78315-99-8

Structure of 78315-99-8

Chemical Structure| 78315-99-8

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Product Details of [ 78315-99-8 ]

CAS No. :78315-99-8
Formula : C6H8O5
M.W : 160.12
SMILES Code : O=C(O)CC(CC(OC)=O)=O
MDL No. :MFCD20638257
InChI Key :VJMSLYCJGYWASX-UHFFFAOYSA-N
Pubchem ID :416086

Safety of [ 78315-99-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 78315-99-8 ]

* 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 [ 78315-99-8 ]

[ 78315-99-8 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 67-56-1 ]
  • [ 10521-08-1 ]
  • [ 78315-99-8 ]
YieldReaction ConditionsOperation in experiment
for 1.0h; To a flask containing 50 g (0.39 mol) of <strong>[10521-08-1]acetonedicarboxylic acid anhydride</strong> was added 160 ml of cold dry MeOH. The monomethylester solution was allowed to stand for 1 h and filtered.. The filtrate of acetonedicarboxylic acid monomethyl ester was used directly in the following condensation reaction.
20 mmol of <strong>[10521-08-1]2,4,6-trioxotetrahydropyrane</strong> were stirred in 30 mL methanol till dissolution and afterwards cooled to -20 C. 20 mmol of the corresponding amine and 40 mmol pyridine-2-carboxaldehyde dissolved in 20 mL methanol, respectively, were added to the solution in parallel in a way that the reaction temperature does not exceed - 20 C. After stirring for 2 h at -10 C the solvent was removed in vacuo at room temperature. The obtained residue was covered with a small amount of methanol and the product crystallized at 4 C. The analytical and spectroscopic data of 19-24 are in accordance with the ref. 30,31,32,33 Methyl (2'R,6'S)-1'-benzyl-4'-hydroxy-1',2',5',6'-tetrahydro-2,2';6',2''-terpyridine-3'-carboxylate (19): C24H23N3O3 (401.5 g/mol), yield: 33% (53%)31, mp. 155 C (163-164).33
at 5 - 20℃; <strong>[10521-08-1]acetonedicarboxylic acid anhydride</strong> (31.4 kg) was added to methanol (100 L) cooled to 5 C. upon vigorous stirring. The resulting solution was kept at ambient temperature for 45 min to ensure that formation of acetone dicarboxylic acid monomethyl ester was complete.
  • 3
  • [ 332-77-4 ]
  • [ 10521-08-1 ]
  • [ 78315-99-8 ]
  • [ 593-51-1 ]
  • 6-methoxy-2-methoxycarbonyl-8-azabicyclo[3.2.1]octane-3-one [ No CAS ]
  • 7-methoxy-2-methoxycarbonyl-8-azabicyclo[3.2.1]octane-3-one [ No CAS ]
  • 7β-hydroxy-2-methoxycarbonyl-8-azabicyclo[3.2.1]octane-3-one [ No CAS ]
  • 6β-hydroxy-2-methoxycarbonyl-8-azabicyclo[3.2.1]octane-3-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium acetate; In methanol; water; for 48.0h;pH 4.5 - 4.9; To a 3 L flask with 53.6 g (0.41 mol) of 2,5-dimethoxydihydrofuran was added 1000 ml of 3N HCl solution.. The mixture was left to stand for 12 h at room temperature and then neutralized with ice-cold NaOH solution (equal moles) at 0 C. To this red solution, was added 41.3 g (0.62 mol) of methylamine hydrochloride in 300 ml H2O, the preformed methanol solution of the monomethylester (50 g (0.39 mol) of acetone dicarboxylic acid anhydride in 160 ml of methanol) and 50 g of sodium acetate in 200 ML of H2O. The mixture (PH 4.5) was stirred for 2 days and the acidity decreased to PH 4.9.. The red solution was extracted with hexane (450 ml*2) to remove nonpolar by-products.. The aqueous solution was basified first with NaOH (1N) to neutral PH, then with potassium carbonate.. sodium chloride (about 200 g) was added.. The saturated solution was extracted with CH2Cl2 (250 ml*8), then with a mixed solvent (t-butyl:1,2-dichloroethane, 37:63, 250 ml*8).. The CH2Cl2 extracted was dried over K2CO3 and solvent was removed to provide 19.6 g of a crude mixture which was separated by column chromatography (SiO2, 10% Et3N, 30-90% EtOAc in hexane and 10% methanol in EtOAc) to afford 7.5 g of 6(7)-methoxy-2-methoxycarbonyl-8-azabicyclo(3.2.1)octane-2-one as an oil and 7 g of 6(7)-hydroxy-2-methoxycarbonyl-8-azabicyclo-(3.2.1)octane-2-one as a crystalline solid.
 

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