Home Cart Sign in  
Chemical Structure| 343773-22-8 Chemical Structure| 343773-22-8

Structure of 343773-22-8

Chemical Structure| 343773-22-8

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 343773-22-8 ]

CAS No. :343773-22-8
Formula : C9H11NO4
M.W : 197.19
SMILES Code : O=C(NO)C1=CC=CC(OC)=C1OC

Safety of [ 343773-22-8 ]

Application In Synthesis of [ 343773-22-8 ]

* 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 [ 343773-22-8 ]

[ 343773-22-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 343773-22-8 ]
  • [ 6299-67-8 ]
YieldReaction ConditionsOperation in experiment
89% General procedure: To a mixture of N-hydroxy-2,6-dimethoxybenzamide (1a) (0.237 g, 1.2 mmol), K2CO3 (0.166 g, 1.2 mmol), and DMSO (0.5 mL) was added acetic anhydride (1.1 mL,0.012 mmol) and heated to 50 C. After stirring at that temperature for 10 min, the reaction mixture was cooled to 0 C and then treated with 2 M HCl (ca. 2mL). After the mixture became the clear solution, 2 M NaOH (ca. 2 mL) was added and extracted with Et2O (15 mL x 3). The combined organic layers were dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/Et2O, 1:1) to yield 2,6-dimethoxyaniline (2a) (0.171 g, 93%) as a white crystalline solid.
General procedure: CDI (0.486 g, 3.0 mmol) was added to a solution of p-toluic acid (0.272 g, 2.0 mmol) in dry DMSO (2 mL), then stirring for 1 h. DMAP (0.122 g, 1.0 mmol) and NH2OTMS (0.420 g, 4.0 mmol) were added to the reaction mixture and stirred at room temperature for 18 h. K2CO3 (0.552 g, 4.0 mmol) was added and the resulting mixture was heated to 90 C. After stirring at that temperature for 3 h, the reaction mixture was cooled to 0 C and then was treated with 2 M HCl (ca. 2 mL). After the mixture became the clear solution, 2 M NaOH (ca. 3 mL) was added and extracted with CH2Cl2 (15 mL 3). The combined organic layerwas dried over anhydrous Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/Et2O, 1:1) to yield p-toluidine (2a) (0.180 g, 79%)
 

Historical Records

Technical Information

Categories