cyclopropyl bromide

—
Reaction #6313
SiO2
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCN=Cc1c(C2CC2)cc(C(F)(F)F)cc1C(F)(F)F
Reaction #67706
Butyl-[1-(2-cyclopropyl-4,6-bis-trifluoromethyl-phenyl)-methylidene]-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1cccc(OC2CC2)c1
Reaction #70287
expected product
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccccc1SC1CC1
Reaction #157745
1-(cyclopropylsulfanyl)-2-methylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Brc1cccc(SC2CC2)c1
Reaction #157762
title compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc2c(c1)OCCN2C1CC1
Reaction #159742
4-Cyclopropyl-3,4-dihydro-2H-benzo[1,4]oxazine
Ausbeute 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1ccc(SC2CC2)cc1
Reaction #183365
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-n2nc(C(=O)C3CC3)cc2-c2ccc(CCNC(N)=O)cc2)cc1
Reaction #195819
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccccn1)C1CC1
Reaction #226130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc2c(c1)C(CCCBr)=CCC2
Reaction #230049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccccc1F)C1CC1
Reaction #233281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(OC(F)F)cc1)C1CC1
Reaction #248382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1cccc(OC2CC2)c1
Reaction #249648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)OCCC(C)(O)C1CC1
Reaction #261360
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccncc1)C1CC1
Reaction #296270
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1cnn(C2CC2)c1
Reaction #307666
1-Cyclopropyl-1H-pyrazole-4-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)Cc1ccc2c(c1)C(O)(C1CC1)c1sccc1CO2
Reaction #330931
captioned compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
c1cc(CC2CC2)ccn1
Reaction #338983
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=Cc1c(C2CC2)cccc1C1CC1
Reaction #341717
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cccc(C2CC2)c1C=O
Reaction #341733
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
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