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Chemical Structure| 100377-63-7 Chemical Structure| 100377-63-7

Structure of 100377-63-7

Chemical Structure| 100377-63-7

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Product Details of [ 100377-63-7 ]

CAS No. :100377-63-7
Formula : C8H10N2O3
M.W : 182.18
SMILES Code : COC1=CC(C(NN)=O)=CC=C1O
MDL No. :MFCD00017076
InChI Key :AWVJTGNFMZKXDN-UHFFFAOYSA-N
Pubchem ID :468601

Safety of [ 100377-63-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 100377-63-7 ]

* 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 [ 100377-63-7 ]

[ 100377-63-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 617-05-0 ]
  • [ 100377-63-7 ]
YieldReaction ConditionsOperation in experiment
73% With hydrazine hydrate; In ethanol; water;Reflux; General procedure: Hydrazides (30-58) were synthesized by one pot conventionalmethod24 Benzoic acid or its derivative (10 mmol) was dissolvedin ethanol (20 mL). Sulfuric acid (3 N, 2 mL) was added and thereaction contents were refluxed for six hours. The reaction wasmonitored with TLC. After the completion of the reaction, the reactionmixture was neutralized by adding solid NaHCO3, and filteredto remove excess of NaHCO3. In the neutralized reaction mixture which contains ethyl ester, hydrazine monohydrate (1.5 mL,3 mmol) was added and refluxed for 3-6 h to complete the reaction.Ethanol and unreacted hydrazine were removed by distillationupto 1/3 volume. The reaction contents were cooled, filteredand recrystallized from methanol to obtain the desired hydrazidecrystals (see Supporting information).
With hydrazine hydrate; In ethanol; for 20h;Reflux; A stirred solution of compound 2 (50 mmol) in ethanol (50 mL) was treated with 85% hydrazine hydrate (20 mL), under reflux for 20 h. After cooling, removal of the solvent under reduced pressure gave a crude product, which was filtered off and purified by washing with saturated NaCl (40 mL) together with small quantity of ethanol to give compound 3.
 

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