Pages
(Move to ...)
Home
ABOUT ME
DIMENSIONS IN NMR SPECTROSCOPY
13 C NMR
1H NMR
CHEMDOODLE/INTERACTIVE SPECT PREDICT
Animations
HELP ME
Multinuclear NMR Spectroscopy
Examples of 13C NMR
Books on NMR spectroscopy
UV-Visible Spectroscopy
IR SPECTRA EXAMPLES
Journals
Organic spectroscopy site
Spectroscopy sites
IR SPECTROSCOPY
Books-2
Recommended Web Sites for Spectra and Spectrum-rel...
DISCLAIMER
Mössbauer spectroscopy
FINDING CHEMICAL SPECTRA
Mass Spectrometry
NMR Overview
Characterisation of Organic Compounds
SDBS Spectral Database System for Organic Compounds
CHEMICAL SHIFT
MASS SPECTROSCOPY
Books-1
MASSBANK PORTAL
11B NMR
▼
Pages
(Move to ...)
Home
ABOUT ME
DISCLAIMER
Organic spectroscopy site
Spectroscopy sites
Journals
Recommended Web Sites for Spectra and Spectrum-related Information
Books-1
Books-2
MASS SPECTROSCOPY
IR SPECTROSCOPY
1H NMR
13 C NMR
SDBS Spectral Database System for Organic Compounds
FINDING CHEMICAL SPECTRA
CHEMICAL SHIFT
Mössbauer spectroscopy
UV-Visible Spectroscopy
Mass Spectrometry
Examples of 13C NMR
Characterisation of Organic Compounds
IR SPECTRA EXAMPLES
NMR Overview
Books on NMR spectroscopy
HELP ME
Multinuclear NMR Spectroscopy
Animations
CHEMDOODLE/INTERACTIVE SPECT PREDICT
DIMENSIONS IN NMR SPECTROSCOPY
MASSBANK PORTAL
▼
(E)-2-(2-(3-Ethoxy-3-oxoprop-1-enyl)-6-fluorophenyl)acetic acid
(E)-2-(2-(3-Ethoxy-3-oxopropyl -1-enyl)-6-fluorophenyl)acetic acid
.
RM,
2-fluorophenylacetic acid (1a )
N -acetyl isoleucine, (3077-46-1)
ethyl acrylate (2a )(451-82-1)
TLC (hexanes:EtOAc:HOAc, 66:33:1) Rf = 0.29;
M.p = 97-99 °C;
1 H NMR (600 MHz, CDCl3 ) δ: 1.33 (t, J = 7.2 Hz, 3 H), 3.87 (d, J = 1.8 Hz, 2 H), 4.27 (q, J = 6.6 Hz, 2 H), 6.38 (d, J = 15.6 Hz, 1 H), 7.10 (t, J = 9.6 Hz, 1 H), 7.29 (td, J 1 = 8.4, J 2 = 6.0 Hz, 1 H), 7.38 (d, J = 7.8 Hz, 1 H), 7.84 (d,J = 15.6 Hz, 1 H);
predict
13 C NMR (150 MHz, CDCl3 ) δ: 14.2, 30.5 (d, J C-F = 5.1 Hz), 60.9, 116.5 (d, J C-F = 22.7 Hz), 120.5 (d, J C-F = 16.1 Hz), 122.1, 122.5 (d, J C-F = 3.2 Hz), 129.1 (d, J C-F = 9.0 Hz), 136.3 (d, J C-F = 3.5 Hz), 140.3 (d, J C-F = 3.4 Hz), 161.4 (d, J C-F = 245.6 Hz), 166.5, 175.9;
Decoupled 19 F NMR (375 MHz, CDCl3 ) δ: -115.11 (s, 1 F);
IR (film): 2984, 1735, 1705, 1638, 1574, 1462, 1369, 1318, 1264, 1241, 1183, 1156, 1001, 971, 866, 802 cm-1 ;
HRMS (ESI-TOF) m/z calcd for C13 H14 FO4 [M+H]+ : 253.0876, found: 253.0871;
Anal. calcd. for C13 H13 FO4 : C 61.90, H 5.20, F 7.53, found: C 62.07, H 5.36, F 7.42.
/////////
No comments:
Post a Comment