Home Cart Sign in  
Chemical Structure| 204452-94-8 Chemical Structure| 204452-94-8

Structure of 204452-94-8

Chemical Structure| 204452-94-8

*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 [ 204452-94-8 ]

CAS No. :204452-94-8
Formula : C12H17BrO3
M.W : 289.17
SMILES Code : CCOC(OCC)COC1=CC(Br)=CC=C1

Safety of [ 204452-94-8 ]

Application In Synthesis of [ 204452-94-8 ]

* 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 [ 204452-94-8 ]

[ 204452-94-8 ] Synthesis Path-Downstream   1~3

  • 1
  • copper(l) cyanide [ No CAS ]
  • [ 204452-94-8 ]
  • [ 17450-68-9 ]
  • [ 95333-17-8 ]
  • 2
  • [ 557-21-1 ]
  • [ 204452-94-8 ]
  • [ 95333-17-8 ]
YieldReaction ConditionsOperation in experiment
30% A mixture of C1-1c and C1-1d (5 g, 25.1 mmol), zinc cyanide (4.2 g, 37.7 mmol) was sequentially added to a 100 mL three-necked flask. Tetrakistriphenylphosphine palladium (2.9 g, 2.5 mmol) and anhydrous N,N-dimethylformamide (50 mL). The reaction mixture was heated and stirred at 100 C for 18 hours under nitrogen. After cooling to room temperature, 200 mL of water was added and extracted with ethyl acetate.(200mL x 3). The combined organic phases were washed twice with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified on silica gel (petroleum ether: ethyl acetate = 100: 1), to give benzofuran-4-carbonitrile C1-1e (1.1g, 30% yield) as a pale yellow solid. The conversion product of C1-1d was separated and removed in this step.
30% In a 500 mL single-necked flask, bromo-3- (2,2-diethoxyethoxy) benzene C1-1b (21 g, 72.6 mmol), 150 mL of toluene, and polyphosphoric acid (10.68 g, 108.93 mmol) were sequentially added. The reaction solution was heated at 95 C and stirred for 4 hours. After cooling to room temperature, the reaction solution was quenched with 1 L of ice water, and extracted with ethyl acetate (500 mL × 3). The combined organic phases were washed twice with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give a total of 5 g of a crude mixture of C1-1c and C1-1d. Step 3: Intermediate benzofuran-4-carbonitrile (C1-1e)In a 100 mL three-necked flask were added a mixture of C1-1c and C1-1d (5 g, 25.1 mmol), zinc cyanide (4.2 g, 37.7 mmol),Tetratriphenylphosphine palladium (2.9g, 2.5mmol)And anhydrous N, N-dimethylformamide (50 mL). The reaction mixture was heated and stirred at 100 C for 18 hours under nitrogen. After cooling to room temperature, 200 mL of water was added and extracted with ethyl acetate (200 mL X 3).The combined organic phases were washed twice with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified on silica gel (petroleum ether: ethyl acetate = 100: 1) to give benzofuran-4-carbonitrile C1-1e (1.1 g, 30% yield),As a pale yellow solid. The conversion product of C1-1d is separated and removed in this step.
1.1 g In a 500 mL single-necked flask, bromo-3- (2,2-diethoxyethoxy) benzene C1-1b (21 g, 72.6 mmol), 150 mL of toluene, and polyphosphoric acid (10.68 g, 108.93 mmol) were sequentially added. The reaction solution was heated at 95 C and stirred for 4 hours.After cooling to room temperature, the reaction solution was quenched with 1 L of ice water, and extracted with ethyl acetate (500 mL × 3). The combined organic phases were washed twice with brine, dried over anhydrous sodium sulfate, filtered,Concentration under reduced pressure gave a crude mixture of C1-1c and C1-1d of 5 g.In a 100 mL three-necked flask were added a mixture of C1-1c and C1-1d (5 g, 25.1 mmol), zinc cyanide (4.2 g, 37.7 mmol),Tetratriphenylphosphine palladium (2.9 g, 2.5 mmol) and anhydrous N, N-dimethylformamide (50 mL).The reaction mixture was heated and stirred at 100 C for 18 hours under nitrogen.After cooling to room temperature, 200 mL of water was added and extracted with ethyl acetate (200 mL X 3).The combined organic phases were washed twice with brine, dried over anhydrous sodium sulfate, filtered,Concentrated under reduced pressure. The residue was purified on silica gel (petroleum ether: ethyl acetate = 100: 1),Benzofuran-4-carbonitrile C1-1e (1.1 g, 30% yield) was obtained as a pale yellow solid.The conversion product of C1-1d is separated and removed in this step.
  • 3
  • [ 204452-94-8 ]
  • [ 95333-17-8 ]
 

Historical Records