Home Cart Sign in  
Chemical Structure| 6919-62-6 Chemical Structure| 6919-62-6

Structure of 6919-62-6

Chemical Structure| 6919-62-6

*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 [ 6919-62-6 ]

CAS No. :6919-62-6
Formula : C5H11NO3
M.W : 133.15
SMILES Code : O=C(N(C)OC)OCC
MDL No. :MFCD00075530

Safety of [ 6919-62-6 ]

Application In Synthesis of [ 6919-62-6 ]

* 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 [ 6919-62-6 ]

[ 6919-62-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24134-09-6 ]
  • [ 6919-62-6 ]
  • bis(1,2-dimethyl-1H-imidazol-5-yl)methanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
A solution of n-BuLi (2.66 M in hexane, 19.5 mL, 51.9 mmol) in THF (100 mL) was stirred under argon at ?-70 C. while a solution of <strong>[24134-09-6]5-bromo-1,2-dimethyl-1H-imidazole</strong> (9.13 g, 52.2 mmol) in THF [60 mL; containing 3 A molecular sieves (18 g)] was added dropwise over 8 minutes via cannula. After stirring for another 4 minutes at ?-70 C., neat ethyl methoxy(methyl)carbamate (2.96 mL, 22.7 mmol) was added dropwise over 3 minutes. This mixture was stirred at ?-70 C. for an additional 5 minutes, and the cold bath was then removed and the slurry was allowed to warm to room temperature with stirring for 1.5 hours. The reaction was then quenched with 5 M aqueous NH4Cl (15 mL), dried (Na2SO4), filtered, and concentrated under high vacuum at 80 C. The resulting orange gummy residue was triturated with hot heptane (?40 mL) and the decanted supernatant was allowed to crystallize to provide impure title compound. This was recrystallized from toluene (?30 mL) to provide, after washing the off-white crystalline filter cake with toluene (2*?3 mL), the title compound as an off-white crystalline solid.
Intermediate 11: bis(1,2-dimethyl-1H-imidazol-5-yl)methanone A solution of -RuLi (2.66 M in hexane, 19.5 mL, 51.9 mmol) in THF (100 mL) was stirred under argon at-70 C while a solution of 5-bromo-l ,2-dimethyI-lH-imidazole (9.13 g, 52.2 mmol) in TFIF [60 mL; containing 3A molecular sieves (18 g)] was added dropwise over 8 minutes via cannula. After stirring for another 4 minutes at ~-70 C, neat ethyl metboxy(methyl)carbamate (2.96 mL, 22.7 mmol) was added dropwise over 3 minutes. This mixture was stirred at-70 C for an additional 5 minutes, and the cold bath was then removed and the slurry was allowed to warm to room temperature with stirring for 1.5 hours. The reaction was then quenched with 5 aqueous NH4C1 (15 mL), dried (Na2S04), filtered, and concentrated under high vacuum at 80 C, The resulting orange gummy residue was triturated with hot heptane (-40 mL) and the decanted supernatant was allowed to crystallize to provide impure title compound. This was recrystallized from toluene (-30 niL) to provide, after washing the off-white crystalline filter cake with toluene (2 x ~3 mL), the title compound as an off-white crystalline solid.
 

Historical Records