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CAS No. : | 345965-52-8 | MDL No. : | MFCD07374439 |
Formula : | C10H9BrO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | BYJIXWOWTNEVFO-UHFFFAOYSA-N |
M.W : | 241.08 | Pubchem ID : | 16227966 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
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* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | With thionyl chloride In methanol at 0 - 70℃; | To a 50 mL round-bottom flask was added l-(4-bromophenyl)cyclopropane-1- carboxylic acid 149a (2 g, 8.30 mmol, 1.00 equiv.) and methanol (20 mL). Thionyl chloride(2.96 g, 24.88 mmol, 3.00 equiv.) was added drop·wise with stirring at 0°C. The resultingmixture was stined at 70 °C ovemight. After cooling to room temperature, the reaction wasquenched by the addition of water/ice. The aqueous mixture was extracted with ethyl acetate5 (50 mL x 2). The combined organic extracts were vvashed with brine (50 rnL x 2, dried overanhydrous sodium sulfate, and concentrated under vacuum. The crude product was purifiedby Flash-Prep-HPLC eluting with EA/PE (from 0percent to 10percent '.vithin 20 rnin) to give methyl1-(4-bromophenyl)cyclopropa.ne-l-carboxyate 149b (l.7g, 80percent;) as colorless oil |
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