Identification | Back Directory | [Name]
(2,2,6,6-tetramethyl-3,6-dihydro-2H-pyran-4-yl)boronic acid, pinacol ester | [CAS]
1142363-56-1 | [Synonyms]
(2,2,6,6-tetramethyl-3,6-dihydro-2H-pyran-4-yl)boronic acid, pinacol ester 2,2,6,6-TetraMethyl-3,6-dihydro-2H-pyran-4-boronic acid pinacol ester, 97% 4,4,5,5-tetramethyl-2-(2,2,6,6-tetramethyl-3H-pyran-4-yl)-1,3,2-dioxaborolane 2,2,6,6-tetramethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyran 4,4,5,5-tetraMethyl-2-(2,2,6,6-tetraMethyl-3,6-dihydro-2H-pyran-4-yl)-1,3,2-dioxaborolane 2H-Pyran, 3,6-dihydro-2,2,6,6-tetramethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- | [Molecular Formula]
C15H27BO3 | [MDL Number]
MFCD11044439 | [MOL File]
1142363-56-1.mol | [Molecular Weight]
266.18 |
Chemical Properties | Back Directory | [Boiling point ]
281.9±50.0 °C(Predicted) | [density ]
0.97±0.1 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [form ]
solid | [Appearance]
White to off-white Solid | [InChI]
InChI=1S/C15H27BO3/c1-12(2)9-11(10-13(3,4)17-12)16-18-14(5,6)15(7,8)19-16/h9H,10H2,1-8H3 | [InChIKey]
VOXXPMAJNSVUKJ-UHFFFAOYSA-N | [SMILES]
C1(C)(C)OC(C)(C)C=C(B2OC(C)(C)C(C)(C)O2)C1 |
Hazard Information | Back Directory | [Synthesis]
(b) 2,2,6,6-tetramethyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyran-1-yl 1,2,2,3,3,4,4,4-ninafluorobutane-1-sulfonate (43.8 g, 0.100 mol) was dissolved in anhydrous dimethoxyethane (DME, 500 mL ), bis(pinacolato)diboron (27.9 g, 0.109 mol), 1,1'-bis(diphenylphosphino)ferrocene (1.60 g, 2.90 mmol), and potassium acetate (KOAc, 29.4 g, 0.30 mol) were added sequentially. After degassing by sonication under argon protection, a 1:1 complex of [1,1'-bis(diphenylphosphino)-ferrocene]-palladium(II) dichloride with dichloromethane (2.19 g, 2.68 mmol) was added. The reaction mixture was heated and stirred at 80 °C overnight. After completion of the reaction, it was cooled to room temperature and filtered through a diatomaceous earth pad. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (eluent: 0-2% ethyl acetate/hexane) to afford (2,2,6,6-tetramethyl-3,6-dihydro-2H-pyran-4-yl)boronic acid pinacol ester as a white solid (17 g, 64% yield).1H-NMR (CDCl3; 400 MHz): δ 6.40 (t, 1H, J = 1.8 Hz), 1.97 (d, 2H, J = 1.8 Hz), 1.21 (s, 12H), 1.18 (s, 6H), 1.13 (s, 6H). | [References]
[1] Patent: US2009/105296, 2009, A1. Location in patent: Page/Page column 44 |
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