methoxyethoxymethyl chloride

COCCOCOc1cc2ccc(-c3ccc(C(=O)OC)cc3)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1231
expected compound
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCCOCOc1c(C(C)(C)C)nc(C)nc1C(C)(C)C
Reaction #6438
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COCCOCOc1ccc(I)cc1
Reaction #6705
4-Methoxyethoxymethoxy-iodobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCCOCOc1ccc(I)cc1
Reaction #11294
4-Methoxyethoxymethoxy-iodobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCCOCOc1ccc([N+](=O)[O-])c(C=O)c1
Reaction #57289
2
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COCCOCC(CC(=O)NC(C)C)(CC1(C(=O)N[C@H]2CCc3ccccc3N(CC(=O)OC(C)(C)C)C2=O)CCCC1)C(=O)O
Reaction #60633
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COCCOCN1C(C)=C(C(=O)OC)C(c2cccc([N+](=O)[O-])c2)C(C(=O)OC)=C1C
Reaction #62678
1-(2-methoxyethoxy)methyl-2,6-dimethyl-3,5-di(carbomethoxy)-4-(3-nitrophenyl)-1,4-dihydropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COCCOCOc1ccc(-c2ccc(/C=C/C(=O)OC)cc2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #69999
(E)-3-[3′-adamantan-1-yl-4′-(2-methoxyethoxymethoxy)-biphenyl-4-yl]-acrylic acid methyl ester
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCCOCN(c1ccc(F)c(C(C)=O)c1F)S(=O)(=O)c1cc(F)ccc1F
Reaction #74174
N-(3-acetyl-2,4-difluoro-phenyl)-2,5-difluoro-N-(2-methoxy-ethoxymethyl)-benzene-sulfonamide
Yield 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCCOCOc1ccc(C=O)nc1
Reaction #81380
5-[(2-methoxyethoxy)methoxy]-2-pyridinecarboxaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCOC(=O)C12CC3CC(CC(OCOCCOC)(C3)C1)C2
Reaction #193112
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCOCOc1ccc([N+](=O)[O-])cc1
Reaction #193329
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(C)OCOCC(C)CCCC1(C)OCCO1
Reaction #214746
6,6-ethylenedioxy-1-methoxyethoxymethoxy-2-methylheptane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
COCCOCOc1ccc(Br)cc1C(F)(F)F
Reaction #253028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCCOCOc1ccc(CCOC(C)=O)cc1OC
Reaction #261683
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCCOCOCCN(C(=O)OCc1ccccc1)C(=O)C(N)Cc1ccccc1
Reaction #267101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C1(COCCOC)CCN(C(=O)OC(C)(C)C)CC1
Reaction #303245
title compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COCCOCO[C@@H]1CC[C@@]2(C)[C@H](CC[C@@H]3[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)CCC=O)CC[C@@H]32)C1
Reaction #310629
3α-(β-methoxyethoxymethoxy)-5β-cholane-24-aldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
COCCOCN(c1onc(C)c1C)S(=O)(=O)c1ccc(Br)s1
Reaction #321498
colorless oil
Yield 56.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
COCCOCOCCc1cccs1
Reaction #357838
title compound
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
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