Alternatived Products of [ 38348-83-3 ]
Product Details of [ 38348-83-3 ]
CAS No. : | 38348-83-3 |
MDL No. : | MFCD00624876 |
Formula : |
C10H10BrNO
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | - |
M.W : | 240.10 g/mol |
Pubchem ID : | - |
Synonyms : |
|
Application In Synthesis of [ 38348-83-3 ]
* 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 [ 38348-83-3 ]
- 1
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[ 616-45-5 ]

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[ 89598-96-9 ]

-
[ 38348-83-3 ]
Yield | Reaction Conditions | Operation in experiment |
90% |
|
General procedure: Aryl boronic acid (1.0 mmol), CuI (5 molpercent),amide (3.0 mmol), and DMSO (1.0 mL) were added to a reactionvial, and the mixture was stirred at room temperature for10 min. A 70percent aqueous solution of TBHP (1.1 mmol) was addedto the reaction mixture dropwise over 5 min. The reaction vialwas then immersed in a preheated oil bath and the progress ofreaction was followed by TLC. Upon completion of reaction, thecooled mixture was partitioned between water and ethyl acetate.The aqueous layer was further extracted with ethyl acetate,and the combined organic layers were washed with brine,dried over Na2SO4, filtered, and concentrated in vacuo. Theresidue was purified by column chromatography on silica gel(hexane?ethyl acetate) to give the desired N-aryl lactam |
- 2
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[ 84964-24-9 ]

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[ 38348-83-3 ]
Yield | Reaction Conditions | Operation in experiment |
56% |
With oxone; oxygen; copper diacetate; potassium iodide; In acetonitrile; at 80℃; under 760.051 Torr; for 12h;Schlenk technique; |
Add 1i (0.5 mmol, 120 mg) to a 10 mL Shrek tube,Acetonitrile (5mL),Anhydrous copper acetate (1mmol, 181mg),Potassium iodide (1mmol, 166mg)And Oxone (615 mg, 1 mmol),After evacuating with oxygen (1 atm), it was placed in an 80 C oil bath and stirred for 12 h.Then, the reaction was quenched by adding 10 mL of saturated brine.It was extracted with ethyl acetate (10 mL × 3).Filter, spin dry, and separated on silica gel column (petroleum ether / ethyl acetate = 3 / 1)Product 2i (67 mg, 56%) was obtained as a white solid. |