2-fluoroethanol

FCCOCc1cccc(Br)c1
Reaction #58861
1-bromo-3-(2-fluoroethoxymethyl)benzene
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NS(=O)(=O)c1ncccc1OCCF
Reaction #83826
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccc(C(C)C)cc1N1CCc2nc(-c3c(C)ccc4[nH]nc(C)c34)nc(OCCF)c2C1
Reaction #168034
2-(3,5-dimethyl-1H-indazol-4-yl)-4-(2-fluoroethoxy)-6-(5-isopropyl-2-methylphenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)CCC(C(O)CF)[N+](=O)[O-]
Reaction #181578
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2cc(-c3ccnc(OCCF)n3)sc2c1
Reaction #184425
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCN(c2ccc(COCCF)cc2)CC1
Reaction #186318
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3C(O)CC2(C)C1C(=O)C(=O)O
Reaction #199931
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)CC(C(O)CF)[N+](=O)[O-]
Reaction #263783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)CC(C(O)CF)[N+](=O)[O-]
Reaction #268393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
FCCOc1cncc(Cl)n1
Reaction #285458
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1cccc(OCc2ccc(Cl)cc2F)c1OCCF
Reaction #337894
compound
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=Cc1cccc(OCc2ccc(Cl)cc2F)c1OCCF
Reaction #340606
compound
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=Cc1cccc(OCc2ccc(Cl)cc2F)c1OCCF
Reaction #381432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCNC(=O)C(C)c1ccc(C#Cc2cnc(OCCF)nc2)cc1
Reaction #418023
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=Cc1ccc(OCCF)cc1
Reaction #426696
4-(2-Fluoroethoxy)benzaldehyde
Yield 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1ccc(S(=O)(=O)OCCF)cc1
Reaction #426741
title compound
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOC(=O)c1cc(F)c2c(c1Cl)C(OCCF)CCS2
Reaction #431052
4-(2-fluoroethoxy)-5-chloro-6-ethoxycarbonyl-8-fluorothiochroman
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=S(=O)(OCCF)C(F)(F)F
Reaction #493944
2-fluoroethyl trifluoromethanesulfonate
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CNc1cc(OCCF)c(C(=O)Nc2ccc(F)c(Cl)c2)cc1[N+](=O)[O-]
Reaction #497304
N-(3-chloro-4-fluorophenyl)-2-(2-fluoroethoxy)-4-methylamino-5-nitro-benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)(C)OC(=O)N1CCN(c2ccc(COCCF)cc2)CC1
Reaction #539482
tert-butyl 4-(4-((2-fluoroethoxy)methyl)phenyl)piperazine-1carboxylate
Yield 22.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
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