1-(2-Vinyl-pyridin-3-yl)propanal O-methyloxime and 1-(6-Vinyl-pyridin-3-yl)propanal O-methyloxime

Vittorio E. Caprio; Michael W. Jones; Margaret A. Brimble

doi:10.3390/M201

,

and

Department of Chemistry, The University of Auckland, Private Bag 92019, Auckland, New Zealand

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Author to whom correspondence should be addressed.

Molecules2001, 6(3), M201;https://doi.org/10.3390/M201

This article belongs to the Section Molbank Section of Molecules, 1997-2001

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The general part of the experimental section [1] has been presented elsewhere. Boron trifluoride diethyl etherate (313 mg, 2.21 mmol) was added dropwise to a solution of oxime 1 (100 mg, 0.735 mmol) in toluene (8 mL) at -78^oC under nitrogen and the mixture stirred for 5 min. Vinylmagnesium bromide (1 M in THF) (2.2 mL, 2.20 mmol) was added dropwise over 10 min and the resultant orange coloured solution stirred at -78°C for 1.5 h [2]. Water (1 mL) was added and the reaction warmed to room temperature. The mixture was extracted with ethyl acetate (3 x 15 mL), dried over magnesium sulfate and concentrated under reduced pressure to give a dark red solid. Further purification by flash chromatography using diethyl ether-hexane (1:9) gave the title compounds 2 (9 mg, 8%) and (3) (14 mg, 10%) as pale yellow oils.

1-(2-Vinyl-pyridin-3-yl)propanal O-methyloxime 2

IR (neat): 2917s, 2847m, 1696m, 1627bm, 1460m, 1054m.

¹H NMR (200 MHz, CDCl₃): 1.23 (3H, t, J 7.8 Hz, H3), 2.67 (2H, q, J 7.8 Hz, H2), 4.08 (3H, s, OCH₃), 5.54 (1H, dd, J 1.9 Hz, J 10.8 Hz, H2″A), 6.26 (1H, dd, J 1.9 Hz, J 17.4 Hz, H2″B), 6.82 (1H, dd, J 10.8 Hz, J 17.4 Hz, H1″), 7.35 (1H, m, H5'), 8.06 (1H, bs, H4'), 8.66 (1H, d, J 2.0 Hz, H6').

EI-MS: 190 (M⁺, 23%), 189 ((M-H)⁺, 28%), 159 (100%), 144 (87%), 136 (10%), 91 (12%), 77 (15%).

Anal. Calc. For C₁₁H₁₄N₂O, 190.1106; found M⁺ 190.1103.

1-(6-Vinyl-pyridin-3-yl)propanal O-methyloxime 3

IR (cm^-1, CH₂Cl₂): 3053m, 2972m, 2938m, 1452m, 1422m, 1265s, 1054s, 739b, 705s.

¹H NMR (200 MHz, CDCl₃): 1.24 (3H, t, J 7.6 Hz, H3), 2.67 (2H, q, J 7.6 Hz, H2), 4.01 (3H, s, OCH₃), 5.56 (1H, dd, J 1.9 Hz, J 10.8 Hz, H2″A), 6.28 (1H, dd, J 1.9 Hz, J 17.0 Hz, H2″B), 7.06 (1H, dd, J 10.8 Hz, J 17.0 Hz, H1″), 7.87 (1H, d, J_4',5' 2.2 Hz, H5'), 8.39 (1H, s, H2'), 8.45 (1H, d, J_4',5' 2.2 Hz, H4').

EI-MS: 190 (M⁺, 26%), 189 ((M-H)⁺, 28%), 159 (100%), 144 (84%), 130 (11%), 117 (10%), 77 (15%).

Anal. calc. for C₁₁H₁₄N₂O (M⁺), 190.1106; found M⁺ 190.1099.

Supplementary materials

Supplementary File 1Supplementary File 2Supplementary File 3Supplementary File 4

References

Brimble, M. A.; Duncalf, L. J. Molecules 2000, 5, 162–166. [CrossRef]
Dieter, R.K.; Datar, R. Can. J. Chem. 1993, 71, 814–823.

Sample availability: available from the authors.

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