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CAS No. : | 2646-90-4 | MDL No. : | MFCD00010327 |
Formula : | C7H4F2O | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | VVVOJODFBWBNBI-UHFFFAOYSA-N |
M.W : | 142.10 | Pubchem ID : | 137663 |
Synonyms : |
|
Signal Word: | Danger | Class: | 3 |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | 1989 |
Hazard Statements: | H225-H315-H319-H335 | Packing Group: | Ⅲ |
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 |
---|---|---|
24% | Dissolved ferf-butyl (5-bromothiazol-2-yl)carbamate (0.5 g, 1 .79 mmol) in tetrahydrofuran (8.95 ml_ ) and cooled to -78 C. Carefully added n-butyllithium (1 .6M in hexanes, 1 .14 ml_, 2.86 mmol) and stirred for 10 minutes, followed by 2,5-difluorobenzaldehyde (271 uL, 2.50 mmol). Stirred at -78 C for 3 h. Warmed to room temperature and quenched with saturated aqueous ammonium chloride (15 ml_). Extracted with ethyl acetate (20 ml_) and washed with brine (15 ml_). The combined organic layers were dried over sodium sulfate, filtered, and concentrated. Purified reaction by column chromatography (eluting with 0-50% ethyl acetate/hexanes through 24 g of silica gel) to give ferf-butyl (5-((2,5-difluorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate as a yellow solid (150 mg, 0.438 mmol, 24%). 1 H NMR (300 MHz, Chloroform-d) d 7.37 (d, J = 3.0 Hz, 1 H), 7.17 (s, 1 H), 7.10 - 6.92 (m, 2H), 6.27 (s, 1 H), 1 .53 (s, 9H). |
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