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CAS No. : | 42580-42-7 | MDL No. : | MFCD00013249 |
Formula : | C9H4F6O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | PINBPLCVZSKLTF-UHFFFAOYSA-N |
M.W : | 258.12 | Pubchem ID : | 736187 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
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 |
---|---|---|
Oakwood Products, Inc., 1741 Old Dunbar Road, West Columbia, S.C. 29172, USA. TCI America, 9211 N. Harborgate Street, Portland, Oreg. 97203, USA 2,5-Bis(trifluoromethyl)benzoic acid; 3,4-bis-trifluoromethyl-benzoic acid; 2-bromobenzoic acid; 3-bromobenzoic acid; 5-bromo-2-chlorobenzoic acid; 5-bromo-4-chloro-2-fluorobenzoic acid; 4-bromo-2,6-difluorobenzoic acid; 2-bromo-3-fluorobenzoic acid; 2-bromo-5-fluorobenzoic acid; ... |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
EXAMPLE 7 2,5-Bis(trifluoromethyl)benzoylguanidine hydrochloride: colorless crystals, m.p. 240 to 242 C. from <strong>[42580-42-7]2,5-bis(trifluoromethyl)benzoic acid</strong> in accordance with variant A. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
69% | 2,5-Bis(trifluoromethyl)benzoic acid (80.3 mg, 0.31 mmol) was dissolved in dry DMF (1.0 mL) and DIPEA (90 muL, 0.58 mmol), HOBt (21.2 mg, 0.156 mmol), EDC (59.6 mg, 0.31 mmol) were added.The reaction mixture was stirred at room temperature for 5 minutes.Dibenzyl (5-aminopentane-1,4-diyl)(S)-dicarbamate (Intermediate A) (100 mg, 0.26 mmol) was added at room temperature and the reaction was continued to stir overnight. The reaction mixture was then diluted with ethyl acetate and washed with saturated NaHCO3 and brine.The organic layer was dried over sodium sulfate and filtered.Filtrate was then concentrated and purified using an ISCO chromatograph with silica (hexane/ethyl acetate) to give the product (113 mg, 69% yield).1H NMR (CDCl3) (300 MHz) delta 7.82 (m, 3H), 7.30 (m, 10H), 5.05 (s, 4H), 4.87 (m, 1H), 3.88 (m, 1H), 3.55 (m, 2H), 3.24 (m, 2H), 1.63 (m, 4H). |
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