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inquiryTIANFU-CHEM - Coumarin 102 Application:TIANFU-CHEM - Coumarin 102
Coumarin 102 cas 41267-76-9Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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8-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine) but-2-ynoate
coumarin 102
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; (triphenylphosphine)gold(I) chloride In 1,4-dioxane; 1,2-dichloro-ethane at 20℃; Reagent/catalyst; Sealed tube; regioselective reaction; | 91% |
With C64H108AuClN2O33 In water at 37℃; for 42h; Reagent/catalyst; Inert atmosphere; Schlenk technique; regioselective reaction; | 52% |
8-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine) 5-(tert-butoxycarbonylamino)hex-2-ynoate
coumarin 102
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; (triphenylphosphine)gold(I) chloride In 1,4-dioxane; 1,2-dichloro-ethane at 20℃; Reagent/catalyst; Sealed tube; regioselective reaction; | 90% |
Conditions | Yield |
---|---|
With triisopropoxytitanium(IV) chloride In toluene for 16h; Pechmann condensation; Reflux; | 73% |
Conditions | Yield |
---|---|
With sulfuric acid at 130℃; for 0.2h; Irradiation; | 62% |
morpholine
formaldehyd
coumarin 102
8-Methyl-9-morpholin-4-ylmethyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With acetic acid | 92% |
coumarin 102
9-bromo-8-methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With N-Bromosuccinimide In acetonitrile for 0.166667h; | 88% |
With N-Bromosuccinimide In acetonitrile |
coumarin 102
9-Chloro-8-methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With copper dichloride In acetonitrile for 0.5h; Heating; | 85% |
coumarin 102
2,3,6,7-tetrahydro-9-methyl-10-iodo-1H,5H-quinolizino<9,9a,1-gh>coumarin
Conditions | Yield |
---|---|
With pyridine; iodine In 1,4-dioxane | 82% |
coumarin 102
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
With trichlorophosphate for 1.083h; Inert atmosphere; | 80.8% |
formaldehyd
coumarin 102
N-methyl-1-octadecylamine
8-Methyl-9-[(methyl-octadecyl-amino)-methyl]-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With acetic acid | 72% |
formaldehyd
coumarin 102
1-amino-2-propene
9-Allylaminomethyl-8-methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With acetic acid | 68% |
formaldehyd
coumarin 102
benzylamine
9-(Benzylamino-methyl)-8-methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With acetic acid | 66% |
formaldehyd
coumarin 102
3-(Benzylamino-methyl)-7-diethylamino-4-methyl-chromen-2-one
9-{[Benzyl-(7-diethylamino-4-methyl-2-oxo-2H-chromen-3-ylmethyl)-amino]-methyl}-8-methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With acetic acid at 75℃; for 1.5h; | 36% |
coumarin 102
iodobenzene
8-Methyl-9-phenyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
In acetonitrile Quantum yield; Irradiation; Et3N; | 35% |
With triethylamine In acetonitrile Irradiation; | 35% |
styrene
coumarin 102
1-endo-phenyl-12b-methyl-1,2,6,7,10,11-hexahydro-3H,5H,9H--cyclobutabenzopyrano<6,7,8-ij>quinolizin-3-one
Conditions | Yield |
---|---|
In acetonitrile for 10h; Irradiation; | 32% |
In acetonitrile Quantum yield; Irradiation; |
coumarin 102
ethyl bromoacetate
(8-Methyl-10-oxo-2,3,5,6-tetrahydro-1H,4H,10H-11-oxa-3a-aza-benzo[de]anthracen-9-yl)-acetic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In acetonitrile Irradiation; | 29% |
2-iodo-propane
coumarin 102
10-isopropyl-9-methyl-2,3,6,7-tetrahydro-1H,5H,11H-chromeno<6,7,8-i,j>quinolizin-11-one
Conditions | Yield |
---|---|
With triethylamine In acetonitrile Irradiation; | 20% |
coumarin 102
9-Fluoro-8-methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
Conditions | Yield |
---|---|
With xenon difluoride In acetonitrile at 0℃; for 0.5h; | 20% |
formaldehyd
coumarin 102
9-(Benzylamino-methyl)-8-methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-one
C41H43N3O4
Conditions | Yield |
---|---|
With acetic acid at 75℃; for 1.5h; | 16% |
Conditions | Yield |
---|---|
With triethyloxonium fluoroborate 1) CH2Cl2, 30 deg C, 20-30 min, 2) 2-3h, reflux; Yield given. Multistep reaction; |
coumarin 102
bis(heptafluorobutyryl) peroxide
10-(heptafluoropropyl)-2,3,6,7-tetrahydro-9-methyl-1H,5H,11H-pyrano<2',3'-4,5>benzo<1,2,3-ij>quinolizine-11-one
Conditions | Yield |
---|---|
In dichloromethane; 1,1,2-Trichloro-1,2,2-trifluoroethane for 4h; Heating; | 15 % Turnov. |
coumarin 102
sodium acetylacetonate
3-(8-Methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-ylidene)-pentane-2,4-dione
Conditions | Yield |
---|---|
With triethyloxonium fluoroborate 1). 40 min. 20 deg C, 2)4 hrs. 50 deg C; Yield given. Multistep reaction; |
coumarin 102
sodium diethylmalonate
2-(8-Methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-ylidene)-malonic acid diethyl ester
Conditions | Yield |
---|---|
With triethyloxonium fluoroborate 1). 40 min. 20 deg C, 2)4 hrs. 50 deg C; Yield given. Multistep reaction; |
coumarin 102
sodium ethyl acetylacetate enolate
2-[8-Methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-(10Z)-ylidene]-3-oxo-butyric acid ethyl ester
Conditions | Yield |
---|---|
With triethyloxonium fluoroborate 1). 40 min. 20 deg C, 2)4 hrs. 50 deg C; Yield given. Multistep reaction; |
coumarin 102
indan-1,3-dione sodium salt
2-(8-Methyl-2,3,5,6-tetrahydro-1H,4H-11-oxa-3a-aza-benzo[de]anthracen-10-ylidene)-indan-1,3-dione
Conditions | Yield |
---|---|
With triethyloxonium fluoroborate 1). 40 min. 20 deg C, 2)4 hrs. 50 deg C; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With triethyloxonium fluoroborate 1) CH2Cl2, 30 deg C, 20-30 min, 2) 2-3h, reflux; Yield given. Multistep reaction; |
coumarin 102
C41H43N3O4
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 66 percent / glacial acetic acid 2: 16 percent / acetic acid / 1.5 h / 75 °C View Scheme |
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