chloromethyl ethyl ether

CCOCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #2092
7-Benzyl-1-ethoxymethyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCn1c(C(N)=O)c(OC(C)C)c2cc(OC)ccc21
Reaction #49878
1-ethoxymethyl-5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamide
Ausbeute 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOCOC(=O)c1c(I)cc(I)c(NC(C)=O)c1I
Reaction #56528
product
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOCC(O)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60293
desired product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #64096
liquid
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOCOC(=O)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #66305
ethoxymethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOCn1cccn1
Reaction #74607
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-]
Reaction #74686
(Ethoxymethyl)triphenylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[CH2]OCC
Reaction #165395
title compound
Ausbeute 66.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOCOC(=O)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #175074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCn1cnc(SC)n1
Reaction #175428
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCCOC(=O)C1=C(C)N(COCC)C(C)=C(C(=O)OCCOCC)C1c1cccc([N+](=O)[O-])c1
Reaction #196922
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCn1c(C(N)=O)c(OC(C)C)c2cc(OC)ccc21
Reaction #199625
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCN(C(=O)CCl)c1c(OC)cccc1OC
Reaction #208107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCSc1ccc([N+](=O)[O-])c(N)c1
Reaction #209114
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCn1c(Br)c(Br)c(S(=O)(=O)C(F)(F)F)c1-c1ccc(Cl)cc1
Reaction #216804
title product
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
—
Reaction #216826
ethyl acetate hexanes
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCOCn1ccnc1
Reaction #221012
1-ethoxymethyl-1H-imidazole
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOCOC1=C(c2cc(Cl)ccc2C(F)(F)F)S(=O)(=O)Cc2nccnc21
Reaction #222245
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOCOc1ccc2occc2c1
Reaction #240995
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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