Ethyl 4-chloroacetoacetate

CCOC(=O)CC(=O)COCC1OC(C)(C)OC1COCC(=O)CC(=O)OCC
Reaction #1344
title compound
Ausbeute 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC(=O)COCC1COC(C)(C)O1
Reaction #1345
title compound
Ausbeute 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1=C(CCl)N2CCOC2(C)C(C(=O)OC)C1c1ccccc1Cl
Reaction #1350
title compound
Ausbeute 17.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)Cc1coc(-c2ccccc2)n1
Reaction #4495
ethyl 2-phenyl-4-oxazoleacetate
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(=O)Cc1csc(C2CCCCC2)n1
Reaction #4496
ethyl 2-cyclohexyl-4-thiazoleacetate
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=c1cc(CCl)c2ccc(O)cc2o1
Reaction #43923
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)Cc1csc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)n1
Reaction #71792
title compound
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)CC(O)CCl
Reaction #77181
4-chloro-3-hydroxybutyric acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)Cc1csc(-c2ccccc2O)n1
Reaction #81854
4a
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1cc(CCl)c2cc(F)c(O)c(F)c2o1
Reaction #91172
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1cn2c(=O)cc(CCl)nc2s1
Reaction #92916
7-chloromethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Oc1cc(CCl)nc(C(Cl)(Cl)Cl)n1
Reaction #95000
crude product
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)CC(=O)CSC(C)(C)C
Reaction #164679
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cc1coc(C2CC2)n1
Reaction #169391
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)CC(=O)COCCn1c(C)ccc1C
Reaction #180634
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C=C(N)CCl
Reaction #185978
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)CSC(C)(C)C
Reaction #197830
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)CON=C(c1ccc(OC)cc1)c1ccc(OC)cc1
Reaction #206618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)COC1CCN(C)CC1
Reaction #206979
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)COCCN=[N+]=[N-]
Reaction #209059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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