反応 #1994301

ord-59b0d7fe5a5c4f5d87e597c2be4d8746

反応方程式

CCOC(=O)C(=O)CC(=O)/C=C/c1ccc(Cl)cc1
(E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid ethyl ester
CCOC(=O)C(=O)CC(=O)/C=C/c1ccc(Cl)cc1
(E)-6-(4-Chlorophenyl)-2,4-dioxo-hex-5-enoic acid ethyl ester
CC(=O)[O-].[NH4+]
ammonium acetate
CCOC(=O)/C(N)=C/C(=O)/C=C/c1ccc(Cl)cc1
(2Z,5E)-2-amino-6-(4-chlorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester
収率 86.0%
CCOC(=O)/C(N)=C/C(=O)/C=C/c1ccc(Cl)cc1
(2Z,5E)-2-Amino-6-(4-chlorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester
収率 86.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

Using the procedure of Example 4, (E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid ethyl ester (4; 79.5 g, 0.284 mol) and ammonium acetate (43.78 g, 0.568 mol) were allowed to react in EtOH (795 mL) to provide (2Z,5E)-2-amino-6-(4-chlorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester (8; 47 g, 86%) as a yellow solid: mp 105-107° C.; 1H NMR (400 MHz, CDCl3) δ 9.40 (br s, 1H), 7.52 (d, J=15.9 Hz, 1H), 7.50-7.47 (m, 2H), 7.38-7.32 (m, 2H), 6.78 (d, J=15.9 Hz, 1H), 6.14 (s, 1H), 6.01 (s, 1H), 4.37 (q, J=7.1 Hz, 2H), 1.39 (t, J=7.1 Hz, 3H); HRMS-ESI (m/z): calcd for C14H14ClNO3, 279.067. found, 279.066.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08598086B2uspto-grants-2013_12