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ChemicalBook CAS DataBase List 1-(4-BROMO-2-THIENYL)ETHAN-1-ONE

1-(4-BROMO-2-THIENYL)ETHAN-1-ONE synthesis

7synthesis methods
-

Yield:7209-11-2 72.6%

Reaction Conditions:

with aluminum (III) chloride;bromine in tetrachloromethane at -40 - 20; for 12.5 h;

Steps:

1 2- Acetyl-4-bromothiophene (M-1)
In 250ml single neck flask of 2-acetyl-thiophene 3.00g (23.81mmol), anhydrous aluminum chloride 9.53g (71.43mmol) and carbon tetrachloride 80ml, cooled to -40 ° C, was slowly dropped stable after 10min bromo 3.81g (23.81mmol) in carbon tetrachloride (20ml), 0.5h drop was completed, stirring at room temperature. 12After h TLC showed the starting material is no longer remaining. The reaction was poured into a saturated NaOH solution and crushed ice, extracted with ethyl acetate (75ml × 3), the combined organic phase was washed twice with saturated brine, dried over anhydrous MgSO 4. Column layer (PE:EA = 500:1), a pale yellow oily liquid 2.74g, 72.6% yield concentrated under reduced pressure.

References:

China Pharmaceutical University;Lu, shuai;Zhang, Liang;Liu, Hai Chun;Guo, xiaoxing;sun, Shan Liang;Chen, Ya Dong;Lu, tao CN103408540, 2016, B Location in patent:Paragraph 0096; 0126; 0127

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