dichloro(methoxy)methane

O=Cc1ccc2c(c1)CCO2
Reaction #3097
title compound
収率 60.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C(O)(C(F)(F)F)C(F)(F)F)ccc1C=O
Reaction #4846
2-methoxy-4-[2,2,2-trifluoro-1-hydroxy-(trifluoromethyl)ethyl]benzaldehyde
収率 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1cc(F)c(C=O)cc1OC
Reaction #6993
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(-c2nc3cccnc3[nH]2)cc1C=O
Reaction #10795
5-(3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethoxy-benzaldehyde
収率 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(-c2c[nH]c(C3CC3)n2)cc1C=O
Reaction #10825
5-(2-cyclopropyl-1H-imidazol-4-yl)-2,4-dimethoxy-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(-c2nncn2CC(C)C)cc1C=O
Reaction #10831
5-(4-isobutyl-4H-[1,2,4]triazol-3-yl)-2,4-dimethoxy-benzaldehyde
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(C)c(C=O)c(O)c1C
Reaction #43908
title compound
収率 40.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1sc2ccccc2c1C=O
Reaction #46512
title compound
収率 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1c(C(C)(C)C)cc(C=O)cc1C(C)(C)C
Reaction #49893
3,5-di-tert-butyl-4-methoxybenzaldehyde
収率 47.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=Cc1cccc2c1OCC2
Reaction #51203
title product
収率 0.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #64050
solid
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCC(=O)C1=C(O)CC(c2c(C)cc(C)c(C=O)c2C)CC1=O
Reaction #64051
2-butyryl-3-hydroxy-5-(3-formyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one
収率 26.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCN(CC)C(=O)N[C@H]1C[C@@H]2c3cc(C=O)cc4[nH]c(Br)c(c34)C[C@H]2N(C)C1
Reaction #64129
2-Bromo-8alpha-(3,3-diethylureido)-6-methyl-ergoline-13-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)CCCCC[C@H](c1ccc(F)cc1)c1c(C)c(C=O)c(C)c(C)c1O
Reaction #65999
methyl (R)-7-(4-fluorophenyl)-7-(3-formyl-6-hydroxy-2,4,5-trimethylphenyl)heptanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1cc(C(C)C)c(C=O)cc1Br
Reaction #66602
5-bromo-2-isopropyl-4-methoxy-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=Cc1c[nH]c(C(=O)C(Cl)(Cl)Cl)c1
Reaction #72534
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=Cc1ccc2c(c1)CCO2
Reaction #82850
title compound
収率 60.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cc(C(C)C)c(C=O)cc1Br
Reaction #168922
5-bromo-2-isopropyl-4-methoxy-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1oc2c([N+](=O)[O-])cccc2c1C=O
Reaction #174640
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)c(-c2c[nH]c(C3CC3)n2)cc1C=O
Reaction #177140
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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