2-hydroxy-benzonitrile

CN(C)C(=S)Oc1ccccc1C#N
Reaction #6100
expected product
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccccc1C#N
Reaction #6137
expected product
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOc1ccccc1C#N
Reaction #8716
colorless liquid
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1ccccc1C#N
Reaction #11356
2-Ethoxybenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CS(=O)(=O)c1ccc(Oc2cc([N+](=O)[O-])c(N)cc2Oc2ccccc2C#N)cn1
Reaction #41570
5-(2-cyano-phenoxy)-4-(6-methanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4ccccn4)nc3cc2Oc2ccccc2C#N)cn1
Reaction #41586
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(C(=O)OCC)C(=O)C(C)Oc1ccc(Oc2ccc(C#N)cc2)cc1
Reaction #63424
desired compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
NC(=S)c1ccccc1O
Reaction #81851
3a
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
N#Cc1cccc(Br)c1O
Reaction #157465
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccccc1Oc1cnn(C2CCCCO2)c(=O)c1Cl
Reaction #200647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC=C(C(=O)OC)c1ccccc1Oc1cc(Oc2ccccc2C#N)ncn1
Reaction #209463
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OC(CBr)COc1ccccc1C#N
Reaction #222881
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1ccccc1C#N
Reaction #236748
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC=C(C(=O)OC)c1ccccc1Oc1cc(Oc2ccccc2C#N)ncn1
Reaction #239623
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccccc1OCCCCl
Reaction #260342
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC=C(C(=O)OC)c1ccccc1Oc1cc(Oc2ccccc2C#N)ncn1
Reaction #284691
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)Oc1ccccc1C#N
Reaction #302729
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#Cc1ccccc1OC1CCNCC1
Reaction #309516
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
N#Cc1ccccc1OCC1CO1
Reaction #312070
oil
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
N#Cc1ccccc1OC1CCNCC1
Reaction #312999
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
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