diethyl ether

C=Cc1ccc(OCCC2OCCCO2)cc1
Reaction #880
2-[2-(4-vinylphenoxy)ethyl]-[1,3]-dioxane
収率 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=Cc1ccc(OCCC2OCCO2)cc1
Reaction #882
2-[2-(4-vinylphenoxy)ethyl]-[1,3]-dioxolan
収率 88.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C=O)c(C)c2c1SCCC2(C)C
Reaction #894
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCC1C(=O)N(C)OC1c1ccccc1
Reaction #907
2-methyl-5-phenyl-4-propargylisoxazolin-3-one
収率 34.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1Br
Reaction #914
title compound
収率 58.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(N)CC.Cl
Reaction #944
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS(=O)(=O)OCC1CCN(C(=N)NC(=O)OCc2ccccc2)C1
Reaction #959
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NCCC1CCN(Cc2ccccc2)C1
Reaction #963
product
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CCCCc1ccccc1
Reaction #974
aldehyde
収率 22.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(N(CC2=CCC(O)(C(C)(C)C)C=C2)C2CCCCC2)ccnc1C
Reaction #1104
4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1159
Ethoxymagnesium Diethylmalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1
Reaction #1176
brown oil
収率 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Br.Cc1ccc(S(=O)(=O)Nc2ccc(NN)c(CC(C)C)c2)cc1
Reaction #1185
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCC(O)CCCCCCCCCCCCC(O)C[N+](C)(C)CC(C)O.[Br-]
Reaction #1203
title compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc[nH]1)C(Cl)(Cl)Cl
Reaction #1223
2-trichloroacetylpyrrole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1cc(I)c[nH]1
Reaction #1224
methyl 4-iodo-2-pyrrolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCCCC12CCCC2
Reaction #1297
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(CC=Cc1ccccc1Br)(C(=O)O)C(=O)O
Reaction #1357
desired product
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C2(C#C[Si](C)(C)C)CCCC(=O)C2)cc1OC1CCCC1
Reaction #1403
3-(3-cyclopentyloxy-4-methoxyphenyl)-3-trimethylsilylethynyl cyclohexan-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCCCC12CCCC2
Reaction #1433
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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