Home Cart Sign in  
Chemical Structure| 904311-38-2 Chemical Structure| 904311-38-2

Structure of 904311-38-2

Chemical Structure| 904311-38-2

*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 [ 904311-38-2 ]

CAS No. :904311-38-2
Formula : C9H6F3NO2S
M.W : 249.21
SMILES Code : N#CC1=CC=C(S(=O)(C)=O)C(C(F)(F)F)=C1
MDL No. :MFCD12196930

Safety of [ 904311-38-2 ]

Application In Synthesis of [ 904311-38-2 ]

* 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 [ 904311-38-2 ]

[ 904311-38-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67515-59-7 ]
  • [ 20277-69-4 ]
  • [ 904311-38-2 ]
YieldReaction ConditionsOperation in experiment
100% In dimethyl sulfoxide; at 80℃; for 22h; <strong>[67515-59-7]4-Fluoro-3-(trifluoromethyl)benzonitrile</strong> (400 mg, 2.12 mmol) was suspended together with sodium methanesulfinate (216 mg, 2.12 mmol) in DMSO (2 ml) and stirred at 800C for 22 hours. The reaction was then cooled, diluted with 25 ml H2O and filtered. Filtered solids were evaporated from toluene to give 536 mg of the title substance (quant).1H NMR (CDCl3) delta 8.49 (d, IH), 8.20 (s, IH), 8.10 (d, IH), 3.24 (s, 3H).
100% In dimethyl sulfoxide; at 80℃; for 22h; 4-(Methylsulfonyl)-3-(trifluoromethyl)benzonitrile <strong>[67515-59-7]4-Fluoro-3-(trifluoromethyl)benzonitrile</strong> (400 mg, 2.12 mmol) was suspended together with sodium methanesulfinate (216 mg, 2.12 mmol) in DMSO (2 ml) and stirred at 80 C. for 22 hours. The reaction was then cooled, diluted with 25 ml H2O and filtered. Filtered solids were evaporated from toluene to give 536 mg of the title substance (quant). 1H NMR (CDCl3) delta 8.49 (d, 1H), 8.20 (s, 1H), 8.10 (d, 1H), 3.24 (s, 3H).
90% In N,N-dimethyl-formamide; at 100℃; for 2h; A mixture of <strong>[67515-59-7]4-fluoro-3-trifluoromethylbenzonitrile</strong> (75 mg, 0.40 mmol), sodium sulfinate (44.5 mg, 0.44 mmol) in N,N-dimethylformamide (1.5 mL) was heated at 100 C. for 2 h. The reaction mixture was cooled to room temperature, quenched with water. The resulting white solid was collected via filtration, washed with cold water, dried in a vacuum oven to give 4-methanesulfonyl-3-trifluoromethyl-benzonitrile (90 mg, 90% yield). This benzonitrile was hydrogenated in 2N NH3 in methanol with 35 mg of Raney Ni under a hydrogen balloon for 2 h. The reaction mixture was filtered through a celite plug, washed with methanol, evaporated in vacuo to give the titled compound.
 

Historical Records

Technical Information

Categories