Issue 8, 1988

3-Hydroxypyrroles and 1H-pyrrol-3(2H)-ones. Part 6. 1H and 13C n.m.r. spectra of 1-substituted, 1,2-disubstituted, and 1,2,2-trisubstituted 1H-pyrrol-3(2H)-ones

Abstract

1 H and 13C n.m.r. parameters of the 1H-pyrrol-3(2H)-one system are discussed. Typical values for the 1-t-butyl derivative (2) are as follows: 2-position, δH 3.70, 4J2.5 0.9 Hz; δc 54.19, 1JCH 141.2, and 3J4–H[=3J5–H] 5.2 Hz; 3-position, δC 199.76, 3J5–H 10.2, 2J4–Hca. 3, and 2J2–Hca. 4.5 Hz; 4-position, δH 5.09, 3J4.5 3.4 Hz; δC 99.13, 1JCH 176.5 and 2J5–H 6.8 Hz; 5-positions, δH 7.93, 3J4.5 3.4 and 4J 0.9 Hz; δC 162.58, 1JCH 173.0, 2J4–H 8.5, and 3J2–H 4.0 Hz The effects of substituents on these parameters are also considered.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1988, 1459-1461

3-Hydroxypyrroles and 1H-pyrrol-3(2H)-ones. Part 6. 1H and 13C n.m.r. spectra of 1-substituted, 1,2-disubstituted, and 1,2,2-trisubstituted 1H-pyrrol-3(2H)-ones

H. McNab and L. C. Monahan, J. Chem. Soc., Perkin Trans. 2, 1988, 1459 DOI: 10.1039/P29880001459

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements