Paracetamol

CC(=O)Nc1ccc(OC(C)(C)C(=O)O)cc1
Reaction #3083
2-(4-acetaminophenoxy)-2-methyl propionic acid
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Nc1ccc(OC(C)(C)C(=O)O)cc1
Reaction #6535
2-(4-acetaminophenoxy)-2-methyl propionic acid
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)Nc1ccc(Oc2cncc(Cl)n2)cc1
Reaction #44563
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(Oc2ccc(NC(C)=O)cc2)cc1
Reaction #51652
methyl 4-(4-acetamidophenoxy)benzoate
Yield 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #54395
crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC1CO1
Reaction #96135
propylene oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)COc1ccc(NC(C)=O)cc1
Reaction #170955
1
Yield 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(C)Oc1ccc(NC(C)=O)cc1
Reaction #170961
8
Yield 27257.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CCCCCOc1ccc(NC(C)=O)cc1
Reaction #170968
15
Yield 42206.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(NC(C)=O)cc1
Reaction #177319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(OS(N)(=O)=O)cc1
Reaction #183170
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(Oc2ccc([N+](=O)[O-])nc2)cc1
Reaction #186049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2c(Oc3ccc(NC(C)=O)cc3)nc(Nc3cc(C)[nH]n3)cc2c1
Reaction #191335
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(OCCCCl)cc1
Reaction #191808
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(Oc2cccc(Br)n2)cc1
Reaction #197658
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(OC(=O)C(Cc2c[nH]cn2)NC(=O)CCNC(=O)CCCBr)cc1
Reaction #212447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(OCC(C)(O)C(=O)Nc2ccc([N+](=O)[O-])c(C)c2)cc1
Reaction #220913
3-(4-Acetylaminophenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(=O)Nc1ccc(OC[C@](C)(O)C(=O)Nc2ccc([N+](=O)[O-])c(C)c2)cc1
Reaction #220919
(2S)-3-(4-Acetylaminophenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(=O)Nc1ccc(OCC(C)(O)C(=O)Nc2ccc(F)c(C)c2)cc1
Reaction #220948
3-(4-Acetylaminophenoxy)-N-(4-fluoro-3-methylphenyl)-2-hydroxy-2-methylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(=O)Nc1ccc(OCCCCCBr)cc1
Reaction #227009
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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