5′-bromo-2′-hydroxyacetophenone

CCOC(=O)COc1ccc(Br)cc1C(C)=O
Reaction #57573
(2-acetyl-4-bromo-phenoxy)-acetic acid ethyl ester
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #59025
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)c1cc(Br)ccc1O2
Reaction #66751
tert-Butyl 6-bromo-4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)c1cc(N2CCN(C)CC2)ccc1O
Reaction #74083
desired product
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)COc1ccc(Br)cc1C(C)=O
Reaction #82227
ethyl (2-acetyl-4-bromophenyl)oxyacetate
Выход 90.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)c1cc(Br)ccc1OCCBr
Reaction #171735
1-[5-bromo-2-(2-bromo-ethoxy)-phenyl]-ethanone
Выход 69.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=NO)c1cc(Br)ccc1O
Reaction #177551
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)COc1ccc(Br)cc1C(C)=O
Reaction #186683
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCC2(CC(=O)c3cc(Br)ccc3O2)C1
Reaction #195393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CC(C)CC2(CC(=O)c3cc(Br)ccc3O2)C1
Reaction #211566
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CC(c2cccc(F)c2)Oc2ccc(Br)cc21
Reaction #221980
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)COc1ccc(Br)cc1C(C)=O
Reaction #234390
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1CC(c2ccccc2F)Oc2ccc(Br)cc21
Reaction #237386
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1CCC2(CC1)CC(=O)c1cc(Br)ccc1O2
Reaction #264363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)CC(=O)c2cc(Br)ccc2O1
Reaction #265411
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1CC(c2ccc(F)cc2)Oc2ccc(Br)cc21
Reaction #268872
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)C1CCC2(CC(=O)c3cc(Br)ccc3O2)C1
Reaction #272259
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1cc(Br)ccc1OC1CCCC1
Reaction #286393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1cc(Br)ccc1OC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #302846
compound 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1ccc(C(=O)Oc2ccc(Br)cc2C(C)=O)cc1
Reaction #302853
compound 13
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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