4-Hydroxyphenethyl alcohol

Oc1ccc(CCOCC2CC2)cc1
Reaction #3090
4-[(2-Cyclopropylmethoxy)-ethyl]-phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS(=O)(=O)OCCc1ccc(OS(C)(=O)=O)cc1
Reaction #7073
1-(Methylsulfonyloxy)-2-[4-(methylsulfonyloxy)phenyl]ethane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCCc1ccc(OCCCBr)cc1
Reaction #42727
title compound
Rendimiento 77.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)C(=O)O
Reaction #62674
oxalic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Oc1ccc(CCOC2CCCCO2)cc1
Reaction #62685
4-(2-tetrahydropyran-2-yloxyethyl)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Oc1ccc(CCCCCCCCOC2CCCCO2)cc1
Reaction #62686
4-(8-tetrahydropyran-2-yloxyoctyl)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=CCc1ccc(O)cc1
Reaction #66041
4-hydroxyphenylacetaldehyde
Rendimiento 49.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
OCCc1ccc(OCCCBr)cc1
Reaction #188939
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NNC(=O)OCCc1ccc(O)cc1
Reaction #210632
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)COc1ccc(CCO)cc1
Reaction #212010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1ccc(Oc2ccc(CCO)cc2)nc1
Reaction #217897
title compound
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Oc1ccc(CCBr)cc1
Reaction #220958
product
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
OCCc1ccc(OCCCCl)cc1
Reaction #231938
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCc1ccc(OCc2ccc(Cl)cc2Cl)cc1
Reaction #238307
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(S(=O)(=O)OCCc2ccc(O)cc2)cc1
Reaction #245435
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)[Si](C)(C)Oc1ccc(CCO)cc1
Reaction #246443
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Oc1ccc(CCO)cc1
Reaction #252129
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)N1CC(COc2ccc(CCO)cc2)OC1c1ccccc1
Reaction #271931
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCCc1ccc(OCc2ccccc2)cc1
Reaction #282853
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)COc1ccc(CCO)cc1
Reaction #294683
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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