Bromomethyl methyl ether

COC12COC(C)(OC1)OC2
Reaction #65110
4-(methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COCc1cnc(SCCC(F)=C(F)F)o1
Reaction #177887
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOP(=O)(COC)OCC
Reaction #216979
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COCc1c(Cl)ccc(Br)c1F
Reaction #247689
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCn1ncc(Cl)c(Cl)c1=O
Reaction #309036
4,5-dichloro-2-methoxymethyl-2H-pyridazin-3-one
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
—
Reaction #357726
ether petroleum ether
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COCOc1c(C)c(C)c2c(c1C)CCC(C)(C(=O)O)O2
Reaction #362639
6-methoxymethoxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COCN1C(=O)C(C(=O)OC)C(c2ccccc2OC)Cc2cc(C(F)(F)F)ccc21
Reaction #390393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COCc1cnc(SCCC(F)=C(F)F)o1
Reaction #438979
5-methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazole
Ausbeute 13.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
COCN1C(=O)CC1SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #442402
oil
Ausbeute 110.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
COCSc1ccc(-c2nc3n(c2-c2ccncc2)CCC3)cc1
Reaction #446899
desired titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
COCOc1cc(OC)ccc1Br
Reaction #452537
title compound
Ausbeute 106.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COCn1c(C)nc2ccc3ccc(C)cc3c2c1=O
Reaction #468782
3,9-dimethyl-2-methoxymethylbenzo[f]quinazolin-1(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COC[N+]1(C)CCCC1.[Br-]
Reaction #470363
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COCOc1cc(OC)ccc1Br
Reaction #486419
title compound
Ausbeute 92410.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
COC[N+]1(C)CCCC1.[Br-]
Reaction #490255
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCN1CCN(c2nc(C)nc3c2nc(-c2ccccc2Cl)n3COC)CC1
Reaction #496004
title compound
Ausbeute 11.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COCOc1ccccc1Br
Reaction #499296
title compound
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC[P+](CC)(CC)COC.[Br-]
Reaction #504133
triethyl(methoxymethyl)phosphonium bromide
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CC[N+](CC)(CC)COC.[Br-]
Reaction #504136
triethyl(methoxymethyl)ammonium bromide
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
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