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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 14, 1984 - Issue 14
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Original Articles

Facile Synthesis of Alkoxyalkyl Cyclopentadienes

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Pages 1305-1312 | Published online: 06 Dec 2006

References

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  • Murata , S. , Suzuki , M. and Noyori , R. 1980 . J. Amer. Chem. Soc. , 102 : 3248 Murata, S.; Suzuki, M.; Noyori, R. Tetrahedron Lett., 1980, 21, 2157; Ojima, I.; Kumagai, M. Chem. Lett., 1978, 575.
  • Ashe , Arthur J. III . 1970 . J. Amer. Chem. Soc. , 92 : 1233 Kraihanzel, Charles S.; Losee, M. L. J. Amer. Chem. Soc., 1968, 90, 4701.
  • Selected Spectral Data: 1 1H NMR (δ, C6D6, 250 MHz) 2.77 (d, J=1.4 Hz, 2H-C); 2.96 (d, J=1.4 Hz, 2H-B); 3.16 (s, 6H-A); 3.17 (s, 6H-B); 3.19 (s, 1H-C); 3.21 (s, 6H-C); 3.22 (s, 1H-B); 3.61 (ddd, J=1.4, 2.8, 8.5 Hz, 1H-A; 3.94 (d, J=8.5 Hz, 1H-A); 6.28–6.64 (m, 4H-A, 3H-B/C). 1A 13C NMR (δ, C6D6, 22.5 MHz) 134.79 (d), 133.24 (d), 104.34 (d), 57.62 (d), 52.74 (q). 1B 13C NMR (δ, C6D6, 22.5 MHz) 133.36 (d), 131.81 (d), 132.31 (d), 130.86(s), 101.48 (d), 52.20 (q), 40.94 (t). 2B 1H NMR (δ, C6D6, 250 MHz) 1.11 (t, J=7.0 Hz, 6H); 3.33–3.60 (m, 5H); 4.03 (d, J=8.4 Hz, 1H); 6.43–6.51 (m, 4H). 13C NMR (δ,C6D6, 22.5 MHz) 135.89 (d), 133.18 (d), 102.95 (d), 61.56 (t), 58.78 (d), 15.43 (q). 3 1H NMR (δ, C6D6, 250 MHz) 0.71 (d, J=6.8 Hz, 3H-B); 0.91 (d, J=6.9 Hz, 3H-C); 1.06 (d, J=6.9 Hz, 3H-C); 1.13 (d, J=6.6 Hz, 3H-B); 1.85 (dsep, J=1.4, 8.1 Hz, 1H-B/C); 2.77 (dd, J=1.3, 23.7 Hz, 1H-B); 2.92 (dd, J=1.3, 23.6 Hz, 1H-B); 3.09 (s, 3H-B); 3.19 (s, 3H-C); 3.44 (d, J=6.9 Hz, 1H-C); 3.46 (d, J=8.2 Hz, 1H-B); 6.29-6.48 (m, 3H-B/C). 3A 13C NMR (δ,C6D6, 22.5 MHz) 148.62 (s), 132.60 (d), 131.69 (d), 131.16 (d), 86.23 (d), 56.43 (q), 39.81 (t), 33.85 (d), 19.54 (q). 4B 1H NMR (δ,C6D6, 250 MHz) 1.00 (s, 6H); 1.08 (t, J=7.0 Hz, 3H); 2.08 (dt, J=7.3, 13.4 Hz, 2H); 2.92 (s, 2H); 3.29 (q, J=7.0 Hz, 2H); 3.75 (s, 1H); 5.04 (d, J=7.8 Hz, 1H); 5.09 (d, J=0.5 Hz, 1H); 5.79–5.96 (m, 1H); 6.29–6.46 (m, 3H). 13C NMR (δ,C6D6, 22.5 MHz) 147.84 (s), 135.99 (d), 132.47 (d), 131.75 (d), 117.04 (t), 85.45 (d), 64.54 (t), 44.52 (t), 42.97 (t), 39.44 (s), 23.83 (q), 23.54 (q), 15.94 (q). 5 1H NMR (δ,C6D6, 250 MHz) 1.04 (s, 6H-A); 1.34 (s, 6H-B); 1.37 (s, 6H-C); 2.88 (d, J=1.1 Hz, 2H-B): 2.95 (s, 3H-B); 3.13 (s, 3H-A); 3.16 (s, 3H-C); 3.24 (d, J=0.7 Hz, 2H-C); 3.31 (s, 1H-A); 6.42 (s, 4H-A and 3H-B/C). 5B 13C NMR (δ,C6D6, 22.5 MHz) 153 (s), 132.53 (d), 131.64 (d), 128.60 (d), 74.25 (s), 50.06 (q), 40.46 (t), 26.93 (q).
  • The amount of TMScp used depended on the amount of the 5-TMS isomer present as determined by 1H NMR. The percentage of this isomer varied from batch to batch.

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