ChemicalBook CAS DataBase List 4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER

4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER synthesis

11synthesis methods

Product Name:4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER
CAS Number:214360-65-3
Molecular formula:C13H16BF3O2
Molecular Weight:272.07

455-14-1
510 suppliers
$5.00/10g

73183-34-3
576 suppliers
$6.00/5g

4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER

214360-65-3
108 suppliers
$9.00/1g

Yield: 86%

Reaction Conditions:

with tert.-butylnitrite;eosin in acetonitrile at 20; for 2 h;Irradiation;

Steps:

General experimental procedure for the synthesis of aryl and hetero-aryl boronates.representative procedure for the synthesis of 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane:
General procedure: tert-Butyl nitrite (155 mg, 1.1 mmol) wasadded drop wise to a mixture of bis(pinacolato)diborane (127 mg, 0.5 mmol),4-anisidine (61 mg, 0.5 mmol) and eosin Y (0.01 mmol) in acetonitrile (3 mL).The resulting mixture was stirred at room temperature under irradiation withblue LED for 2 h (TLC). This mixture after being diluted with ethyl acetate(5 mL) was ltered through celite and the ltrate was extracted with ethylacetate (3 10 mL). The extract was washed with brine, dried over anhydrousNa 2 SO 4 , and evaporated to leave the crude product which was puried bycolumn chromatography over silica gel with hexane-ethyl acetate (98:2) aseluent to furnish pure 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane as a light yellow viscous liquid (3d, 208 mg, 88%); IR (neat)2978, 2933, 2839, 2526, 2050, 1950, 1911, 1724, 1605, 1570 cm1;1H NMR(500 MHz, CDCl 3 ) d 1.33 (s, 12H), 7.82 (s, 3H), 6.89 (d, J = 8.0 Hz, 2H), 7.75 (d,J = 8.0 Hz, 2H);13C NMR (125 MHz, CDCl 3 ) d 24.9 (4C), 55.2, 83.6 (2C), 113.4(2C), 136.6 (2C), 162.3. The spectroscopic data is in full agreement with thosereported for an authentic sample.14This procedure was followed for all thereactions listed in Table 2. All of these products (3a,143b,143c,16a3d,143e,143f,8a3g,143h,143i,143j,8a3k,8a3l,8a3m,143n,8c3o,16b) are known compounds,and their spectroscopic data are in agreement with those previously reported.

References:

Ahammed, Sabir;Nandi, Shiny;Kundu, Debasish;Ranu, Brindaban C. [Tetrahedron Letters,2016,vol. 57,# 14,p. 1551 - 1554]

455-13-0 Synthesis