4-hydroxybenzaldehyde

O=Cc1ccc(OCCC2OCCCO2)cc1
Reaction #879
4-(2-[1,3]-dioxane-2-yl-ethoxy)benzaldehyde
収率 100.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1ccc(OCCC2OCCO2)cc1
Reaction #881
4-(2-[1,3]-dioxolan-2-yl-ethoxy)benzaldehyde
収率 104.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1ccc(OCCCOc2ccc(C=O)cc2)cc1
Reaction #3121
product
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1oc(-c2ccccc2)nc1COc1ccc(C=O)cc1
Reaction #4506
4-(5-methyl-2-phenyl-4-oxazolyl)methoxybenzaldehyde
収率 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=S(=O)(NCCN(CC=Cc1ccc(Cl)cc1)Cc1ccc(O)cc1)c1cccc2cnccc12
Reaction #5840
title compound
収率 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)Oc1ccc(C=C(C(=O)O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #6511
a-p-Nitrophenyl-p-acetoxycinnamic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)Oc1ccc(C=C(C(=O)O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #6516
a-p-Nitrophenyl-p-acetoxycinnamic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=Cc1ccc(OC2CCC2)cc1
Reaction #7472
4-cyclobutyloxybenzaldehyde
収率 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(OCC(F)(F)C(F)(F)F)cc1
Reaction #44759
4-(2,2,3,3,3-pentafluoropropoxy)benzaldehyde
収率 30.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)CCCOc1ccc(C=O)cc1
Reaction #45929
4-(3-diethylaminopropoxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCC(C)Oc1ccc(C=O)cc1
Reaction #50164
4-(1-methylbutyloxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=Cc1ccc(OCCCCl)cc1
Reaction #61972
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Oc1ccc(CN2CCCCC2)cc1
Reaction #61975
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(C=NC2CCN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4-c3ccc(F)cc3)C2)cc1
Reaction #62923
1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-(4-hydroxybenzylidene)amino-1-pyrrolidinyl)-quinoline-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=Cc1ccc(OCCCN2C(=O)c3ccccc3C2=O)cc1
Reaction #63323
title compound
収率 68.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCC[C@H]1CC[C@H](CCCOc2ccc(C=O)cc2)CC1
Reaction #64066
4-[3-(trans-4-pentylcyclohexyl)-1-propyloxy]benzaldehyde
収率 121.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCC[C@H]1CC[C@H](/C=C/COc2ccc(C=O)cc2)CC1
Reaction #64069
4-[(E)-3-(trans-4-pentylcyclohexyl)allyloxy]benzaldehyde
収率 60.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1c(C=O)cccc1-c1ccc2ccccc2n1
Reaction #65975
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)C=Cc1ccc(O)cc1
Reaction #66942
pale yellow solid
収率 70.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)COc1ccc(C=O)cc1
Reaction #68812
solid
収率 92.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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