Home Cart Sign in  
Chemical Structure| 135484-67-2 Chemical Structure| 135484-67-2

Structure of 135484-67-2

Chemical Structure| 135484-67-2

*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 [ 135484-67-2 ]

CAS No. :135484-67-2
Formula : C14H14ClNO3S
M.W : 311.78
SMILES Code : O=S(=O)(NC1C(CO)=CC=C(Cl)C=1)C1C=CC(C)=CC=1
MDL No. :N/A

Safety of [ 135484-67-2 ]

Application In Synthesis of [ 135484-67-2 ]

* 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 [ 135484-67-2 ]

[ 135484-67-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 37585-16-3 ]
  • [ 98-59-9 ]
  • [ 135484-67-2 ]
YieldReaction ConditionsOperation in experiment
With pyridine; In dichloromethane; at 20℃; General procedure: A solution of 4-toluene sulfonyl chloride (4.58 g, 1.2 equiv) or methanesulfonyl chloride (1.9 mL, 1.2 equiv) and pyridine (2 mL, 1.3 equiv) in 20 mL CH2Cl2 was added slowly to the solution of compound 11 (0.02 mol) in 40 mL CH2Cl2. The mixture was stirred overnight at room temperature. Then 30 mL diluted HCl solution was added to the reaction mixture, the organic layer was separated using separating funnel. Subequently, the aqueous phase was extracted with 15 mL CH2Cl2 three times, the combined organic layers were washed separately with saturated NaHCO3 (30 mL) and saturated NaCl (30 mL) three times. The organic layer was dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was purified by column chromatography using petroleum ether/EtOAc = 1/1 to give the product 12.
With pyridine; In dichloromethane; at 20℃; General procedure: The corresponding (2-aminophenyl)methanol (10 mmol) was dissolved in dichloromethane (1.2 M, 8.5 mL) and pyridine (0.809 mL, 10 mmol, 1 eq.) and the corresponding benzenesulfonyl chloride (12 mmol, 1.2 eq.)were added. The reaction was stirred at room temperature until all the starting (2-aminophenyl)methanol was consumed as judged by TLC (typically 8-20 hours). The reaction was concentrated under reduced pressure and triturated with n-hexane to give N-(2-(hydroxymethyl)phenyl)benzenesulfonamides sufficiently pure.
With pyridine; In chloroform; at 20℃; for 2h; General procedure: The product S1 was dissolved in CHCl3. Then pyridine (1.2 equiv) and 4-toluenesulfonyl chloride (1.2 equiv) were added to the solution. The mixture was stirred at room temperature for 2 hours. After the reaction was completed, the reaction mixture was quenched with saturated ammonium chloride, and the mixture was extracted with ethyl acetate and dried over Na2SO4. After removal off the solvent, the crude product S2 was used directly without further purification.
 

Historical Records