2-fluoro-4-hydroxybenzoic acid

—
Reaction #849
acid chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #2453
4-acetoxy-2-fluorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(OCc1ccccc1)c1ccc(OCc2ccccc2)cc1F
Reaction #62173
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1ccc(O)cc1F
Reaction #160126
methyl 2-fluoro-4-hydroxy-benzoate
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCOC(=O)c1ccc(O)cc1F
Reaction #216844
ester
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #261748
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccc(OCc2ccccc2)cc1F
Reaction #292840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #321758
2-fluoro-4-acetoxybenzoic acid
Yield 62.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
COC(=O)c1ccc(O)cc1F
Reaction #327081
title compound
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCCCCCCCCC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #334985
titled compound
Yield 70.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCCCCCCCCC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #334986
titled compound
Yield 59.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
COC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #430442
2-fluoro-4-methoxycarbonyloxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C(O)c1ccc(OCCCCF)cc1F
Reaction #438529
title compound
Yield 39.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #453280
4-acetoxy-2-fluorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #455980
4-acetoxy-2-fluorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=C(O)c1ccc(Oc2nc3ccccc3s2)cc1F
Reaction #471705
title compound
Yield 63.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COC(=O)c1ccc(O)cc1F
Reaction #477556
title compound
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COC(=O)c1ccc(O)cc1F
Reaction #491516
T7.1
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COC(=O)c1ccc(O)cc1F
Reaction #491548
T31.1
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(=O)Oc1ccc(C(=O)O)c(F)c1
Reaction #506011
2-fluoro-4-acetoxybenzoic acid
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
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