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Chemical Structure| 81926-25-2 Chemical Structure| 81926-25-2

Structure of 81926-25-2

Chemical Structure| 81926-25-2

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Product Details of [ 81926-25-2 ]

CAS No. :81926-25-2
Formula : C10H11NO2
M.W : 177.20
SMILES Code : CC(NC1=CC=C(OCC2)C2=C1)=O

Safety of [ 81926-25-2 ]

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 [ 81926-25-2 ]

* 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 [ 81926-25-2 ]

[ 81926-25-2 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 42933-43-7 ]
  • [ 81926-25-2 ]
YieldReaction ConditionsOperation in experiment
With acetic anhydride; In acetic acid; (a) 9.5 g of <strong>[42933-43-7]2,3-dihydrobenzo[b]furan-5-amine</strong> in 40 ml of acetic acid and 10 ml of acetic anhydride is heated to 60° C. for 11/2 hours and concentrated. The residue is recrystallized from aqueous ethanol. Yield: 11.5 g of N-(2,3-dihydrobenzo[b]furan-5-yl)acetamide, mp 96° C.
  • 2
  • [ 75-36-5 ]
  • [ 42933-43-7 ]
  • [ 81926-25-2 ]
  • 3
  • [ 108-24-7 ]
  • [ 64-19-7 ]
  • [ 42933-43-7 ]
  • [ 81926-25-2 ]
YieldReaction ConditionsOperation in experiment
at 60℃; for 12h; Step 3: Preparation of 5-acetylamino-2,3-dihydrobenzofuran [Show Image] The product (5.2 g, 38.5 mmol) obtained in Step 2 was dissolved in AcOH (20 mL) and Ac2O (5 mL), heated to 60°C, reacted for 12 h, and concentrated to obtain a crude product (6 g, 88.0percent).
  • 4
  • [ 108-24-7 ]
  • [ 42933-43-7 ]
  • [ 81926-25-2 ]
YieldReaction ConditionsOperation in experiment
99% With pyridine; In 1,4-dioxane; at 0 - 20℃; for 16h; Ac2O (2 equiv) and pyridine (1 equiv) were added dropwise to a stirred solution of compound 7 or 8, respectively, (1 equiv) in dioxane (4 mL) at 0C and the solution was stirred at 20C for 16 h. The solution was diluted with water (50 mL) and extracted with ethyl acetate (350 mL). The organic layer was washed with brine, dried over MgSO4, and then evaporated to give 9 (99%) as a brown solid or 10 (86%) as a white solid
86% In 1,4-dioxane; at 20℃; for 15h; To a solution of the appropriate amine (1.0mmol) in 1,4-dioxane was added acetic anhydride (2.1mmol) and the mixture was stirred at room temperature for 15h. After completion, the solution was diluted with water and extrated with EtOAc several times. The combined organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography to afford the desired product.
In ethyl acetate; for 0.5h; Step 3: Preparation of 5-amino-6-nitro-2,3-dihydrobenzofuran [Show Image] At room temperature, acetic anhydride (10.3 mL, 110 mmol) was added dropwise to a solution of the product obtained in the Step 2 (12 g, 89 mmol) and ethyl acetate (80 mL), after dropwise addition, acetic anhydride (19 mL) was further added, stirred for 0.5 h. Then concentrated nitric acid (7.6 mL, 110 mmol) was added dropwise into the above reaction solution, cooled to room temperature, filtered to obtain a solid. The reaction mixture of the solid, hydrochloric acid (20 mL) and anhydrous ethanol (40 mL) was refluxed for 4 h, cooled to room temperature, filtrated, washed with water, and dried to obtain a product (9.8 g, 61.3%).
  • 6
  • [ 52022-77-2 ]
  • [ 81926-25-2 ]
 

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