2-chloroethanol

CS(=O)(=O)CS(=O)(=O)OCCCl
Reaction #4821
2-Chloroethyl (Methylsulfonyl)methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
OCCNCc1cccc(F)c1
Reaction #8734
2-(3-fluoro-benzylamino)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCCN(CCO)c1cccc2c1OCCO2
Reaction #9830
crude product
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)c1cc2c(c(C(C)(C)C)c1)OC(=O)C2c1ccc(OCCO)cc1
Reaction #50776
5,7-di-tert-butyl-3-[4-(2-hydroxyethoxy)phenyl]-benzofuran-2-one
Rendimiento 61.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Cc1cc(C(O)C(=O)O)ccc1OCCO
Reaction #50780
4-(2-hydroxyethoxy)-3-methylmandelic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C(NC(COCC1CCN(CCO)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #60707
title compound
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #63574
35
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
ClCCOc1cccc2[nH]ccc12
Reaction #78267
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(OCCO)cc1
Reaction #78790
4-(2-hydroxyethoxy)toluene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
OCCN(CCO)c1cccc2c1OCCO2
Reaction #79481
crude product
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(CCSCCO)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80334
title compound
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(OCCCl)c1cccc(O)c1
Reaction #81037
product
Rendimiento 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CS(=O)(=O)CS(=O)(=O)OCCCl
Reaction #93237
2-Chloroethyl (Methylsulfonyl)methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
OCCOc1cccnc1
Reaction #162656
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
ClCCn1cc(Br)cn1
Reaction #171550
title compound 75
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(S(=O)(=O)OCCCl)cc1
Reaction #172302
2-chloroethyl 4-methylbenzenesulfonate
Rendimiento 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1ccnc1SCCO
Reaction #174807
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCSCCc1ccccn1
Reaction #175077
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCSCCc1ccccc1
Reaction #175367
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc(F)cc1OCCCl
Reaction #176666
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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