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Chemical Structure| 3943-77-9 Chemical Structure| 3943-77-9

Structure of 3943-77-9

Chemical Structure| 3943-77-9

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Product Details of [ 3943-77-9 ]

CAS No. :3943-77-9
Formula : C11H14O4
M.W : 210.23
SMILES Code : O=C(OCC)C1=CC=C(OC)C(OC)=C1
MDL No. :MFCD00015150
InChI Key :AYYNUGSDPRDVCH-UHFFFAOYSA-N
Pubchem ID :77546

Safety of [ 3943-77-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 3943-77-9 ]

* 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 [ 3943-77-9 ]

[ 3943-77-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 3943-77-9 ]
  • [ 41764-74-3 ]
YieldReaction ConditionsOperation in experiment
95% With hydrazine hydrate; In ethanol; for 18h;Reflux; A solution of ethyl 3,4-dimethoxybenzoate (868 mg, 4.13 mmol.) and hydrazine hydrate (64 wt%, 600 µL, 12.4 mmol) in EtOH (0.3 mL) was refluxed for 18 h while stirring. After cooling to rt the solvent was evaporated and the residue was dissolved in water (10 mL). The resulting solution was extracted with EtOAc (10 x 10 mL) and the combined organic extracts were dried over Na2SO4 and evaporated in order to obtain 3,4-dimethoxybenzohydrazide 24 as a colourless solid (770 mg, 3.92 mmol, 95%). Mp. 132.8-134.4 C; 3307, 2939, 2845, 1626, 1500, 1275, 1148, 1073, 957, 635; 1H NMR (300 MHz, DMSO-d6) d 9.62 (s, 1H, NHNH2), 7.44 (dd, J = 8.2, 1.2 Hz, 1H, H6), 7.42 (d, J = 2.0 Hz, 1H, H2), 6.99 (d, J = 8.2 Hz, 1H, H5), 4.42 (s, 2H, NHNH2), 3.79 (s, 6H, C3-OCH3, C4-OCH3) ppm; 13C NMR (76 MHz, DMSO-d6) d 165.5 (CO2NHNH2), 151.0 (C4) 148.1 (C3), 125.4 (C1), 120.0 (C6), 110.8 (C5), 110.1 (C2), 55.5 (C3-OCH3/C4-OCH3), 55.4 (C3-OCH3/C4-OCH3) ppm; MS (ESI+): m/z (%) = 197.4 (100) [M+H]+, 219.3 (22) [M+Na]+. The analytical data are in accordance with the literature. [16]
72.7% With hydrazine hydrate; In ethanol;Reflux; General procedure: A solution of the isolated esters 2a-e (10mmol) in ethanol (20mL), hydrazine hydrate (97%, 3mL) was added and heated under reflux for 5-8h. After cooling, the formed precipitate was filtered off, washed with water, dried, and crystallized from ethanol.
72.7% With hydrazine hydrate; In ethanol;Reflux; General procedure: Hydrazine hydrate (97%, 30 mmol, 1.5 mL) was added to a solutionof the isolated esters 2a-e (10 mmol) in ethanol (20 mL), and themixture was heated at reflux for 5-8 h. After cooling, the resultingprecipitate was filtered off, washed with water, dried, and crystallizedfrom ethanol.
  • 3
  • [ 3943-77-9 ]
  • [ 2024-83-1 ]
  • [ 1521-41-1 ]
YieldReaction ConditionsOperation in experiment
77%; 23% With diisobutylaluminium hydride; ammonium chloride; In tetrahydrofuran; at 66℃; for 16h;Inert atmosphere; General procedure: The solution of aminoalane reagent (prepared from 20 equiv. DIBAL-H in case of ester and lactonesubstrates or from 40 equiv. in case of carboxylic acid and amide substrates) was added to a solutionof carboxylic acid (1 eqiuv.) or its derivative (lactone, ester or amide, 1 equiv.) in anhydrous THF atroom temperature. Stirring was continued for 16 hours at 66 C. After this time, the reaction mixturewas cooled, quenched with aqueous solution of KHSO4 and the product was extracted with CHCl3.The extract was washed with water, dried over anhydrous sodium sulfate, and the solvent was evaporated. The crude product was purified by silica gel chromatography with hexane / ethyl acetateelution.
 

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