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4,4,6-Trimethyl-2-(3,3,3-trifluoroprop-1-en-2-yl)-1,3,2-dioxaborinane

CAS No.: 1011460-68-6

Category

Cat.NO.:A364230  Purity:98% mixed with stabilizer

Product Details of [ 1011460-68-6 ]

CAS No. : 1011460-68-6
Formula :

C9H14BF3O2

M.W :

222.01

SMILES Code :
C=C(B1OC(C)CC(C)(C)O1)C(F)(F)F
MDL No. : MFCD08669623
InChI Key : GGSSZVWESZQFOZ-UHFFFAOYSA-N
Pubchem ID : 16414270

Safety of [ 1011460-68-6 ]

GHS Pictogram:
Signal Word: Warning
Hazard Statements: H302-H312-H332
Precautionary Statements: P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 1011460-68-6 ]

* 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.

  • Downstream synthetic route of [ 1011460-68-6 ]

[ 1011460-68-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1011460-68-6 ]
  • [ 131818-17-2 ]
  • [ 1147098-21-2 ]
Yield Reaction Conditions Operation in experiment
69.4% With potassium carbonate;tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; water; at 20℃; for 7h;Heating / reflux; To a mixture of tert-butyl 4-bromophenylcarbamate (1.67 g, 6.14 mmol), potassium carbonate (3.38 g, 24.46 mmol), and tetrakis(triphenylphosphine)palladium (365 mg, 0.316 mmol), was added 4,4,6-trimethyl-2-(3,3,3-trifluoroprop-1-en-2-yl)-1,3,2-dioxaborinane (1.64 g, 7.39 mmol), and degassed 1,2-dimethoxyethane (40 mL) and water (20 mL). The mixture for refluxed for 2 hours, cooled to ambient temperature, added more of 4,4,6-trimethyl-2-(3,3,3-trifluoroprop-1-en-2-yl)-1,3,2-dioxaborinane (475 mg, 2.14 mmol) and tetrakis(triphenylphosphine)palladium-(189 mg, 0.164 mmol), and refluxed for 5 hours. The reaction mixture was cooled to room temperature, filtered, diluted with water (200 mL), extracted twice with ethyl acetate (200 mL), washed with brine, dried (Na2SO4) and concentrated to an orange oil. The residue was purified by silica gel chromatography (AnaLogix SF25-40G; 50 micron silica; eluted with 0-15% ethyl acetate in hexane at 30 mL/min) to provide the title compound (1.223 g, 4.26 mmol, 69.4% yield) as a yellow solid. 1H NMR (300 MHz, DMSO-d6) delta ppm 9.53 (s, 1H), 7.52 (d, J=8.8, 2H), 7.40 (d, J=8.4, 2H), 6.03-5.99 (m, 1H), 5.97-5.94 (m, 1H), 1.48 (s, 9H); MS (DCI/NH3) m/e 305 (M+NH4)+.
 

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