Home Cart Sign in  
Chemical Structure| 946147-63-3 Chemical Structure| 946147-63-3

Structure of 946147-63-3

Chemical Structure| 946147-63-3

*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 [ 946147-63-3 ]

CAS No. :946147-63-3
Formula : C12H16BrI
M.W : 367.06
SMILES Code : CC(C1=C(I)C(C(C)C)=CC(Br)=C1)C

Safety of [ 946147-63-3 ]

Application In Synthesis of [ 946147-63-3 ]

* 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 [ 946147-63-3 ]

[ 946147-63-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 80058-84-0 ]
  • [ 946147-63-3 ]
YieldReaction ConditionsOperation in experiment
67% With toluene-4-sulfonic acid; potassium iodide; tert-butyl alcohol; sodium nitrite; In water; at 0 - 25℃; for 4h; 4-Bromo-2,6-diisopropylaniline (35.6 g, 138.96 mmol) was added to a suspension of p-TsOH monohydrate (118.95 g, 625.34 mmol) in a mixture of t-BuOH (500 mL) and water (30 mL). Themixture was cooled to 0 C in an ice bath and a solution of sodium nitrite (28.76 g, 416.89 mmol) and potassium iodide (86.51 g, 521.11 mmol) in water (70 mL) was then added dropwise over 2.5 h, keeping the temperature of the mixture at 10-15 C. Following the addition, the temperature was then allowed to rise to 25 C, and the mixture was stirred for an additional 1.5 h. The reaction mixture was poured into water and extracted with Et20. The ether layer was thenwashed with 10% sodium bisulfite solution to remove iodine related by-products. The organic layer was dried over MgSO4 and concentrated under reduced pressure. The residue was flushed through the silica gel plug eluting with hexane / EtOAc (100 / 0 to 90 / 10). Fractions containing the desired product were combined and concentrated under reduced pressure to afford pure 5- bromo-2-iodo-1,3-diisopropylbenzene (34.5 g, 67% yield). LCMS (Method A): 366.0 [M],retention time 4.31 mm.
60 g With sulfuric acid; sodium nitrite; In acetonitrile; at 0 - 20℃; for 1h; To a 2 L 3-neck flask, equipped with mechanical stirrer, thermometer, and additional funnel, added 300 g of ice and 300 mL of H2SO4. <strong>[80058-84-0]2,6-diisopropyl-4-bromoaniline</strong> (46.0 g, 0.18 mol) in 200 mL of CH3CN was added dropwise to this mixture while the temperature was maintained under 5 C. Then sodium nitrite (22.5 g, 0.32 mol) in 180 mL of ice cold water was added dropwise while the temperature was maintained around 0 C. The resulting clear solution was slowly poured into the solution of potassium iodide (105 g, 0.63 mol) in 300 ml of water at room temperature. The mixture was stirred for 1 h. After regular work up, the crude product was distilled at 170 C. under vacuum to afford 1-iodo-2,6-diisopropyl-4-bromobenzene (60 g) as light brown soft solid upon cooling.
60 g With sulfuric acid; potassium iodide; sodium nitrite; In water; acetonitrile; at 20℃; for 1h; Mechanical stirrer, a thermometer and an addition funnel equipped with a 2 ? 3-neck flask was added to ice and H2SO4 in 300 of 300 g. Of the 200 CH3CN 2,6- diisopropyl-4-bromoaniline (46.0 g, 0.18 mol) was added dropwise to the mixture while maintaining the temperature below 5 . 180 ice cooled solution of sodium nitrite in water of (22.5 g, 0.32 mol) and was added dropwise while maintaining the temperature at about 0 . The resulting clear solution to a solution of potassium iodide in water (105 g, 0.63 mol) in 300 slowly poured at room temperature. The mixture was stirred for 1 hour. Conventional work eophu, distilling the crude product under vacuum at 170 1-iodo-2,6-diisopropyl-4-bromobenzene (60 g) was obtained as a light brown soft solid under cooling.
  • 2
  • [ 80058-84-0 ]
  • [ 946147-63-3 ]
  • imidazophenanthridine ligand [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium iodide; sulfuric acid; sodium nitrite; In water; acetonitrile; EXAMPLE 37 General Procedure B for imidazophenanthridine ligand syntheses To a 2 L 3-neck flask, equipped with mechanical stirrer, thermometer, and additional funnel, added 300 g of ice and 300 mL of H2SO4. <strong>[80058-84-0]2,6-diisopropyl-4-bromoaniline</strong> (46.0 g, 0.18 mol) in 200 mL of CH3CN was added dropwise to this mixture while the temperature was maintained under 5° C. Then sodium nitrite (22.5 g, 0.32 mol) in 180 mL of ice cold water was added dropwise while the temperature was maintained around 0° C. The resulting clear solution was slowly poured into the solution of potassium iodide (105 g, 0.63 mol) in 300 ml of water at room temperature. The mixture was stirred for 1 h. After regular work up, the crude product was distilled at 170° C under vacuum to afford 1-iodo-2,6-diisopropyl-4-bromobenzene (60 g) as light brown soft solid upon cooling.
 

Historical Records