3-methoxy-3-methylbutane-1-ol

COC(C)(C)CCOS(=O)(=O)c1ccccc1C(F)(F)F
Reaction #375899
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(C)(C)CCOc1cccc([N+](=O)[O-])c1C#N
Reaction #558880
2-(3-methoxy-3-methylbutoxy)-6-nitrobenzonitrile
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
COC(C)(C)CC=NO
Reaction #562716
N-hydroxy-3-methoxy-3-methylbutan-1-imine
Yield 38.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
COC(C)(C)CCOS(=O)(=O)CC(F)(F)F
Reaction #784484
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(C)(C)CCOc1cccc([N+](=O)[O-])c1C#N
Reaction #799017
2-(3-methoxy-3-methylbutoxy)-6-nitrobenzonitrile
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
COC(C)(C)CCOS(=O)(=O)c1c(F)c(F)c(F)c(F)c1F
Reaction #907505
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(C)(C)CCOS(=O)(=O)c1ccccc1C(F)(F)F
Reaction #1973939
desired product
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
COC(C)(C)CCOS(=O)(=O)c1c(F)c(F)c(F)c(F)c1F
Reaction #1973940
desired product
Yield 163.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
COC(C)(C)CCOS(=O)(=O)CC(F)(F)F
Reaction #1973945
desired product
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
COC(C)(C)CCn1nc(I)c(=O)c2cccc(F)c21
Reaction #2053488
expected compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
COC(C)(C)CCOS(=O)(=O)c1ccc(C)cc1
Reaction #2366152
3-methoxy-3-methylbutyl 4-methylbenzenesulfonate
Yield 49.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09