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CAS No. : | 1261478-26-5 | MDL No. : | MFCD18399428 |
Formula : | C9H7F3O3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | WYAZXWRYHRTDET-UHFFFAOYSA-N |
M.W : | 220.15 | Pubchem ID : | 70874124 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* 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 |
---|---|---|
Multi-step reaction with 2 steps 1: di-isopropyl azodicarboxylate; triphenylphosphine / N,N-dimethyl-formamide / 3 h / 0 °C / Inert atmosphere 2: lithium hydroxide monohydrate / methanol; water / 3 h / 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1: di-isopropyl azodicarboxylate; triphenylphosphine / N,N-dimethyl-formamide / 3 h / 0 °C / Inert atmosphere 2: lithium hydroxide monohydrate / methanol; water / 3 h / 20 °C 3: pyridine; trichlorophosphate / 0.5 h / 0 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
79% | With di-isopropyl azodicarboxylate; triphenylphosphine In N,N-dimethyl-formamide at 0℃; for 3h; Inert atmosphere; | 32.2 [00344] To a mixture of Example 32b (670 mg, 3.05 mmol), Example 32c (710 mg, 3.05 mmol), PPh3 (1.18 g, 4.5 mmol) was added dried DMF (15 mL), and the mixture was degassed for N2 protection. Then, DIAD (1.23 g) was injected into the mixture at 0°C dropwise, and the reaction solution was stirred for 3 h. After extraction with EtOAc (10 mL*2),the combined organic layer was dried over Na2S04,filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (DCM/MeOH = 95/5) to give the desired product Example 32d (1.05 g, yield 79%) ascolorless oil.LCMS [M+l]+ = 436.0 |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
81% | With thionyl chloride at 0 - 65℃; for 5h; | 32.1 [00343] To the solution of Example 32a (900 mg, 4.37 mmol) in Me OH (20 mL) at 0°C was added SOCl2 (1 mL), and the mixture was heated at 65°C for 5 h. After the temperature was cooled down to r.t., it was concentrated under reduced pressure. The residue was purified by silica gel chromatography (pure petroleum ether) to give the desired product Example 32b (780 mg, yield 81%) as colorless liquid. |
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