4-methoxybenzyl chloride

—
Reaction #3327
208
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(Cc1ccc(OC)cc1)OCC
Reaction #5010
Diethyl 4-methoxybenzylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(COC(=O)c2c(SC)sc3c(F)c(F)c(F)cc3c2=O)cc1
Reaction #5455
title compound
Выход 32.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Cl-]
Reaction #6701
4-methoxybenzyltriphenyl phosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(OC)cc1
Reaction #7512
title compound
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(Cn2cc(C(c3ccccc3)N(C)C)c3ccccc32)cc1
Reaction #9125
{[1-(4-Methoxybenzyl)-1H-indol-3-yl]-phenylmethyl}-dimethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(COCc2ccc(Br)cc2)cc1
Reaction #9333
7-2
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(COc2ccc(C(C)=O)c(O)c2)cc1
Reaction #42759
1-[2-Hydroxy-4-(4-methoxy-benzyloxy)-phenyl]ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #43544
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Выход 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #43546
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CSC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)cc1.Cl
Reaction #47052
product 223
Выход 51.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(Cn2cc(I)c(C(=O)Nc3ccccc3)n2)cc1
Reaction #48600
4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide
Выход 71.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #53950
alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(Cn2c(=O)ccn([C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)c2=O)cc1
Reaction #53954
1-[(2R,3R,4R,5R)-3,4-bis{[tert-butyl(dimethyl)silyl]oxy}-5-(hydroxymethyl)tetrahydro-2-furanyl]-3-(4-methoxybenzyl)-2,4(1H,3H)-pyrimidinedione
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(COc2ccc(Br)cc2-c2cc(Nc3ccc(Cl)cc3)nc(N)n2)cc1
Reaction #56937
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(Cn2cc(Br)c(-c3ccc([N+](=O)[O-])cc3)n2)cc1
Reaction #57205
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(CSc2cccc(N)c2)cc1
Reaction #62602
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COc1ccc(Cn2cc(I)cn2)cc1
Reaction #66513
4-iodo-1-(4-methoxybenzyl)-1H-pyrazole
Выход 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(Cn2cc(B3OC(C)(C)C(C)(C)O3)cn2)cc1
Reaction #66515
1-(4-methoxybenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(COc2c(C=O)cccc2C(C)(C)C)cc1
Reaction #69618
24
Выход 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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