Home Cart Sign in  
Chemical Structure| 82330-54-9 Chemical Structure| 82330-54-9

Structure of 82330-54-9

Chemical Structure| 82330-54-9

*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 [ 82330-54-9 ]

CAS No. :82330-54-9
Formula : C9H8ClNO5
M.W : 245.62
SMILES Code : O=CC1=C([N+]([O-])=O)C=C(OC)C(OC)=C1Cl
MDL No. :MFCD00099543

Safety of [ 82330-54-9 ]

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 [ 82330-54-9 ]

* 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 [ 82330-54-9 ]

[ 82330-54-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5417-17-4 ]
  • [ 82330-54-9 ]
YieldReaction ConditionsOperation in experiment
78% With trifluorormethanesulfonic acid; acetic acid; potassium nitrate; at 0 - 20℃; In acetic acid (80 mL)Trifluoromethanesulfonic acid (26.6 mL, 299 mmol) was added to a solution of <strong>[5417-17-4]2-chloro-3,4-dimethoxybenzaldehyde</strong> (20 g, 100 mmol) and potassium nitrate (30.2 g, 299 mmol) with stirring at 0 ° C. The resulting mixture was stirred at room temperature overnight. The reaction mixture was then poured into water and neutralized with saturated aqueous sodium hydrogen carbonate solution. The precipitate was collected by filtration and dried to obtain Compound 155a (19 g, yield 78percent).
56% TRIFLUOROMETHANESULFONIC acid (0.96 ml, 11 mmol) was added to a solution of 2-chloro- 3, 4-DIMETHOXYBENZALDEHYDE (2.0 g, 10 mmol) and potassium nitrate (1.11 g, 11 mmol) in acetic acid (5 ml) with stirring at 0°C under a nitrogen atmosphere, and the resulting mixture was stirred at room temperature for 4 hours under the nitrogen atmosphere. The reaction mixture was then poured into water, neutralized with a saturated aqueous sodium hydrogencarbonate solution and extracted twice with ethyl acetate (100 ml). The combined organic layers were washed with water (80 ml) and a saturated aqueous sodium chloride solution (80 ml) and dried over anhydrous sodium sulfate. After filtration, the solvent was removed in vacuo, and the residue thus obtained was purified by silica gel column chromatography using a 4: 1 by volume mixture of hexane and ethyl acetate as the eluant to yield 2-chloro-3,4-dimethoxy-6-nitrobenzaldehyde as a colorless solid (1.36 mg, yield: 56percent).
With nitric acid; at 0 - 65℃; for 2h; At 0°C nitirc acid (4.5 ml) was slowly added to <strong>[5417-17-4]2-chloro-3,4-dimethoxybenzaldehyde</strong> (500 mg, 2.49 mmol). The reaction mixture was heated to 65°C to solubilize the starting material and then allowed to stir at RT for 2h. The mixture was poored on ice and the precipitate was collected by filtration, rinsed with water and dried under HV to afford the title compound which was used without further purification. LC MS (ESI): 244.1 [M-H].
 

Historical Records

Technical Information

• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Julia-Kocienski Olefination • Kinetics of Alkyl Halides • Knoevenagel Condensation • Kumada Cross-Coupling Reaction • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nomenclature of Ethers • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Ethers • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Ethers • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

Categories