O-benzyl hydroxylamine hydrochloride

—
Reaction #1914
pure product
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CBr)NOCc1ccccc1
Reaction #3059
title compound
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCCCCCCBr)NOCc1ccccc1
Reaction #9178
8-bromo-octanoic acid benzyloxyamide
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Brc1ccc2c(c1)C1(CCCCC1)C(=NOCc1ccccc1)N2
Reaction #9427
5′-bromospiro{cyclohexane-1,3′-[3H]indol}-2′(1′H)-one 2′(O-benzyloxime)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1cc(C(CC(=O)NOCc2ccccc2)N2C(=O)c3ccccc3C2=O)ccc1OC
Reaction #9931
N-benzyloxy-3-(3-ethoxy-4-methoxyphenyl)-3-phthalimidopropionamide
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1cc(C(CC(=O)NOCc2ccccc2)N2C(=O)c3cccc([N+](=O)[O-])c3C2=O)ccc1OC
Reaction #9932
N-benzyloxy-3-(3-ethoxy-4-methoxyphenyl)-3-(3-nitrophthalimido)propionamide
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1cc(C(CC(=O)NOCc2ccccc2)N2Cc3ccccc3C2=O)ccc1OC
Reaction #9933
N-benzyloxy-3-(3-ethoxy-4-methoxyphenyl)-3-(1-oxoisoindolinyl)propionamide
Yield 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1cc(C(CC(=O)NOCc2ccccc2)N2C(=O)c3ccc([N+](=O)[O-])cc3C2=O)ccc1OC
Reaction #9942
N-benzyloxy-3-(3-ethoxy-4-methoxyphenyl)-3-(4-nitrophthalimido)-propionamide
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1cc(F)c(F)c(C=NOCc2ccccc2)c1F
Reaction #10373
3-(benzyloxyiminomethyl)-2,4,5-trifluorobenzoic acid
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CCCC(N)CC1
Reaction #44480
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1cc(C(=O)NOCc2ccccc2)cc(C(=O)OCC)c1
Reaction #51869
white powder
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(S(=O)(=O)NOCc2ccccc2)cc1
Reaction #57444
off-white colored solid
Yield 107.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=S(=O)(CCCCl)NOCc1ccccc1
Reaction #65155
N-benzyloxy-3-chloropropylsulfonamide
Yield 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOc1c(C=NOCc2ccccc2)c(=O)n(C)c(=O)n1C
Reaction #70972
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCSc1c(C=NOCc2ccccc2)c(=O)n(C)c(=O)n1C
Reaction #70978
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C(CCc1nc(-c2ccccc2)c(-c2ccccc2)o1)=NOCc1ccccc1
Reaction #70990
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc2c(c1)c1cc(Br)ccc1n2C/C(COc1ccccc1)=N/OCc1ccccc1
Reaction #90446
white solid
Yield 93.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #170259
solid
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C1=NCC(=NOCc2ccccc2)CN1.Cl
Reaction #217002
white material
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COC(CCCNC(=O)NOCc1ccccc1)OC
Reaction #338186
3-(4,4-dimethoxy-butyl)-1-(benzyloxy)-urea
Yield 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
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