N-(3-hydroxyphenyl)acetamide

COC(=O)c1ccccc1COc1cccc(NC(C)=O)c1
Reaction #1922
methyl 2-(3-acetamidophenoxymethyl)benzoate
Ausbeute 61.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1sccc1COc1cccc(NC(C)=O)c1
Reaction #1925
methyl 3-(3-acetamidophenoxymethyl)-2-thiophenecarboxylate
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Nc1cccc(Oc2cncc(Cl)n2)c1
Reaction #44562
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1ccc(C=O)c(O)c1
Reaction #54949
2-hydroxy-4-acetylaminobenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=NCC(=O)Nc1ccccc1O
Reaction #57306
nitroso acetamidophenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)Nc1cccc(OC2CCN(C)CC2)c1
Reaction #72919
N-[3-(1-Methyl-piperidin-4-yloxy)-phenyl]-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)Nc1cccc(OCCCBr)c1
Reaction #83883
3-(3-acetamidophenoxy)propyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=C(C)CCOc1cccc(NC(C)=O)c1
Reaction #161154
N-[3-(3-methyl-but-3-enyloxy)-phenyl]-acetamide
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)Nc1ccc(C=O)c(O)c1
Reaction #224927
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Nc1cccc(OCCCBr)c1
Reaction #320351
3-(3-acetamidophenoxy)propyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(=O)Nc1cccc(OCCCBr)c1
Reaction #321038
3-(3-acetamidophenoxy)propyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(=O)Nc1cccc(OCCCBr)c1
Reaction #322579
3-(3-acetamidophenoxy)propyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(=O)Nc1cccc(OCCCBr)c1
Reaction #351356
3-(3-acetamidophenoxy)propyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(=O)Nc1cccc(OCCCBr)c1
Reaction #352669
3-(3-acetamidophenoxy)propyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(=O)Nc1cccc(OCCCBr)c1
Reaction #354151
3-(3-acetamidophenoxy)propyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(=O)Nc1cccc(OCC#N)c1
Reaction #374479
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)Nc1cccc(Oc2cc(Nc3ccc4c(c3)CN(C(=O)OC(C)(C)C)CC4)c([N+](=O)[O-])cn2)c1
Reaction #376651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)Nc1cccc(OC(=O)N(C)c2ccccc2)c1
Reaction #403300
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
—
Reaction #414877
white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CCNc1cccc(O)c1
Reaction #416536
compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
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