TBPA

CC1C[NH+](C)C(C)N1C.CCCCOP(=O)([O-])OCCCC
Reaction #159250
1,2,3,4-tetramethylimidazolinium dibutyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)CCC1CN(C(=O)OC(C)(C)C)C(C(OCc2ccccc2)C(Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO1
Reaction #245854
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCOP(=O)([O-])OCCCC
Reaction #289238
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(O)C(=O)[O-].[NH4+]
Reaction #544432
ammonium lactate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
O=C1C=CC(=O)O1
Reaction #1050061
maleic anhydride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
Brc1ccc(C#Cc2ccc(C#Cc3ccccc3)cc2)cc1
Reaction #1056805
4-[4′-(phenylethynyl)phenylethynyl]phenylbromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1.O=C(O)O
Reaction #1093758
bisphenol A polycarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
CC(O)CN.CCCCOP(=O)(OCCCC)OCCCC
Reaction #1277969
TBPA MIPA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
CCCCOP(=O)(OCCCC)OCCCC.NCCOCCOCC(=O)O
Reaction #1277970
TBPA AEEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
CC(N)(CO)CO.CCCCOP(=O)(OCCCC)OCCCC
Reaction #1277971
TBPA AMPD
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
O=S(=O)(c1ccccc1)c1ccccn1
Reaction #1618557
2-benzenesulfonylpyridine
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_03
CCCCOP(=O)([O-])[O-].[Cl][Sb]([Cl])([Cl])([Cl])[Cl]
Reaction #1665339
Antimony Pentachloride Butyl Phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_09
O=S(=O)(c1ccccc1)c1ccccn1
Reaction #1787992
2-benzenesulfonylpyridine
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_02
CC(C)(C)c1cc(-n2nc3ccccc3n2)c(O)c(C(C)(C)C)c1
Reaction #1943600
2-(2-Hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole
収率 85.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_08
CCCCOP(=O)([O-])OCCCC.CCCC[P+](CCCC)(CCCC)CCCC
Reaction #1956796
product
収率 77.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_12
CCCCOP(=O)([O-])OCCCC.CCCC[P+](CC(C)C)(CC(C)C)CC(C)C
Reaction #1956797
product
収率 68.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_12
CCCCOP(=O)([O-])OCCCC.CCCC[N+]1(C)C=CN=C1
Reaction #1956799
product
収率 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_12
O=Cc1cccc2ccccc12
Reaction #2066840
1-naphthaldehyde
収率 25.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_11
O=Cc1cccc2ccccc12
Reaction #2066841
1-naphthaldehyde
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_11
—
Reaction #2066842
starting material
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_11
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