3-nitrophenol

O=[N+]([O-])c1cccc(OCCOCCOCCO)c1
Reaction #5144
2-(2-(2-(3-nitrophenoxy)ethoxy)ethoxy)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=[N+]([O-])c1ccccc1
Reaction #9193
nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)COc1cccc([N+](=O)[O-])c1
Reaction #45250
ethyl 2-(3-nitrophenoxy)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)CCCOc1cccc([N+](=O)[O-])c1
Reaction #45936
N,N-diethyl-N-[3-(3-nitrophenoxy)propyl]amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1cccc(O)c1Cl
Reaction #65143
product
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)c1ccc2cc(Oc3cccc([N+](=O)[O-])c3)ccn2c1=O
Reaction #77190
solid
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CCOc1cccc([N+](=O)[O-])c1
Reaction #95042
3-nitrophenoxyacetonitrile
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)COc1ccc([N+](=O)[O-])cc1
Reaction #158516
ethyl 4-nitrophenoxyacetate
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(C)(C)Oc1cccc([N+](=O)[O-])c1
Reaction #158520
ethyl 2-methyl-2-(3-nitrophenoxy)propanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(C)(Oc1cccc([N+](=O)[O-])c1)C(=O)OCC
Reaction #158528
diethyl 2-methyl-2-(3-nitrophenoxy)malonate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #158529
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)COc1ccc([N+](=O)[O-])cc1
Reaction #163626
ethyl 4-nitrophenoxyacetate
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(C)(C)Oc1cccc([N+](=O)[O-])c1
Reaction #163630
ethyl 2-methyl-2-(3-nitrophenoxy)propanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(C)(Oc1cccc([N+](=O)[O-])c1)C(=O)OCC
Reaction #163637
diethyl 2-methyl-2-(3-nitrophenoxy)malonate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #163638
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)OC[C@@H](COc2cccc([N+](=O)[O-])c2)O1
Reaction #172355
desired product 132
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cccc(OCc2ccc(Br)cc2)c1
Reaction #184961
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cccc(OCCOC2CCCCC2)c1
Reaction #203260
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC(CCOc1cccc([N+](=O)[O-])c1)C(=O)OC1CCCC1
Reaction #208181
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cccc(Oc2nccnc2Cl)c1
Reaction #212377
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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