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inquiryName: 2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde Synonyms: 9-Julolidinecarboxaldehyde CAS:33985-71-6 MF: C13H15NO Appearance:White powder Storage:Store in cool and dry place, away from sun light. Package:25kg Application:OLED o
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inquiryProduct Name: 2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde Synonyms: 9-Julolidinecarboxaldehyde;5H-BENZO(IJ)QUINOLIZINE-9-CARBOXALDEHYDE, 2,3,6,7-TETRAHYDRO-1;2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde;1,2,
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inquiry9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water pH=Ca. 8 - 9; | 98% |
julolidine
N,N-dimethyl-formamide
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-formamide With trichlorophosphate at 20℃; for 0.5h; Vilsmeier-Haack Formylation; Inert atmosphere; Stage #2: julolidine at 90℃; for 4.5h; Vilsmeier-Haack Formylation; Inert atmosphere; | 94% |
Stage #1: N,N-dimethyl-formamide With trichlorophosphate at 2℃; for 0.5h; Stage #2: julolidine at 90℃; for 4h; | 93% |
With trichlorophosphate Vilsmeier reaction; | 92% |
julolidine
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-formamide With trichlorophosphate at 0℃; for 1.25h; Stage #2: julolidine for 1.16667h; Vilsmeier Formylation; | 91% |
Conditions | Yield |
---|---|
With diethyl ether; trichlorophosphate |
1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline hydrobromide
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: trichlorophosphate / 0.75 h / 0 °C 1.2: 0 - 40 °C 2.1: sodium hydroxide / water; methanol / pH Ca. 8 - 9 View Scheme |
2-aminopyridine
9-julolidinecarboxaldehyde
tert-butylisonitrile
Conditions | Yield |
---|---|
With chloroacetic acid In methanol at 100℃; for 1h; Sealed tube; | 98% |
9-julolidinecarboxaldehyde
N,N'-diethyl-2-thiobarbituric acid
Conditions | Yield |
---|---|
In ethanol for 6h; Ambient temperature; | 97% |
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
With acetic anhydride at 90℃; for 8h; Knoevenagel Condensation; | 97% |
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
With acetic anhydride at 90℃; for 8h; Knoevenagel Condensation; | 97% |
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
With pyrrolidine In methanol at 20℃; for 4h; Knoevenagel Condensation; Darkness; Schlenk technique; Inert atmosphere; | 97% |
9-julolidinecarboxaldehyde
cyclopenta-1,3-diene
6-(julolidin-9-yl)fulvene
Conditions | Yield |
---|---|
With pyrrolidine In methanol at 0 - 20℃; Inert atmosphere; | 95% |
piperidine
9-julolidinecarboxaldehyde
N-piperidine julolidine-9-thioamide
Conditions | Yield |
---|---|
With sulfur In N,N-dimethyl-formamide at 200℃; for 0.5h; Willgerodt-Kindler reaction; microwave irradiation; | 93% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol; water at 20℃; for 48h; | 93% |
9-julolidinecarboxaldehyde
(1R,2R)-1,2-diaminocyclohexane
Conditions | Yield |
---|---|
With sodium sulfate In methanol for 6h; Ambient temperature; | 92% |
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
With pyrrolidine In methanol at 20℃; for 2h; Knoevenagel Condensation; Schlenk technique; Inert atmosphere; Darkness; | 92% |
2-Amino-6-bromopyridine
9-julolidinecarboxaldehyde
1-(isocyanomethyl)-4-methoxybenzene
Conditions | Yield |
---|---|
With chloroacetic acid In methanol at 100℃; for 1h; Sealed tube; | 91% |
9-julolidinecarboxaldehyde
9-acetyl-2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol; water at 20℃; for 48h; | 90% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 50℃; for 12h; | 89% |
2-Amino-6-bromopyridine
9-julolidinecarboxaldehyde
Benzyl isocyanide
Conditions | Yield |
---|---|
With chloroacetic acid In methanol at 100℃; for 1h; Sealed tube; | 89% |
9-julolidinecarboxaldehyde
3-(dicyanomethylidene)-2,3-dihydrobenzothiophene-1,1-dioxide
Conditions | Yield |
---|---|
In ethanol for 6h; Ambient temperature; | 88% |
Conditions | Yield |
---|---|
In methanol for 6h; Reflux; | 88% |
9-julolidinecarboxaldehyde
3-(4-methylquinolin-1-ium-1-yl)propane-1-sulfonate
C26H28N2O3S
Conditions | Yield |
---|---|
With pyrrolidine In ethanol Heating; | 87% |
9-julolidinecarboxaldehyde
2,3,5,8-tetramethylbisthiazolo[4,5-e:5',4'-g]-1,3-benzothiazolium iodide
2-[(E)-2-(9-julolidinyl)vinyl]-3,5,8-trimethylbisthiazolo[4,5-e:5',4'-g]-1,3-benzothiazolium iodide
Conditions | Yield |
---|---|
In methanol at 120℃; under 5250.53 Torr; for 1.16667h; Knoevenagel Condensation; Microwave irradiation; | 87% |
9-julolidinecarboxaldehyde
3-(4-methylpyridiniumyl)propane-1-sulfonate
C22H26N2O3S
Conditions | Yield |
---|---|
With pyrrolidine In ethanol Heating; | 86% |
9-julolidinecarboxaldehyde
2,6-diphenyl-4-methyltelluropyrylium tetrafluoroborate
C31H28NTe(1+)*BF4(1-)
Conditions | Yield |
---|---|
With acetic anhydride for 4h; Ambient temperature; | 86% |
9-julolidinecarboxaldehyde
cyclohexylamine
Conditions | Yield |
---|---|
With sodium sulfate In methanol for 6h; Ambient temperature; | 85% |
9-julolidinecarboxaldehyde
2,4,6-trimethylpyrylium tetrafluoroborate
Conditions | Yield |
---|---|
With tetrafluoroboric acid In acetonitrile at 100℃; Microwave irradiation; | 85% |
16-(2-Cyano-acetoxy)-hexadecanoic acid 4-methoxy-benzyl ester
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at 25℃; for 1h; | 85% |
9-julolidinecarboxaldehyde
2,3-dimethylbenzothiazolium iodide
(E)-3-methyl-2-(2-(2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-9-yl)vinyl)benzo[d]thiazol-3-ium iodide
Conditions | Yield |
---|---|
With pyridine In methanol for 12h; Knoevenagel Condensation; Reflux; | 85% |
With piperidine In ethanol | 70% |
2-cyano-N-(prop-2-ynyl)acetamide
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
Stage #1: 9-julolidinecarboxaldehyde With DIMCARB In tetrachloromethane at 20℃; Knoevenagel Condensation; Stage #2: 2-cyano-N-(prop-2-ynyl)acetamide In tetrachloromethane at 20℃; Knoevenagel Condensation; | 85% |
9-julolidinecarboxaldehyde
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at 25℃; for 1h; | 84% |
2-thiazolylamine
9-julolidinecarboxaldehyde
tert-butylisonitrile
Conditions | Yield |
---|---|
In toluene at 100℃; for 0.166667h; Microwave irradiation; Sealed tube; | 84% |
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